GENESYS CROSSFT PFT-55MB

GUDID 10845854028223

GENESYS CROSSFT PUNCH, 5.5MM

Conmed Corporation

Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Orthopaedic broach Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable
Primary Device ID10845854028223
NIH Device Record Keye3dd8958-ce3e-4a04-860e-b46689beba7e
Commercial Distribution StatusIn Commercial Distribution
Brand NameGENESYS CROSSFT
Version Model NumberPFT-55MB
Catalog NumberPFT-55MB
Company DUNS071595540
Company NameConmed Corporation
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY

Device Identifiers

Device Issuing AgencyDevice ID
GS110845854028223 [Primary]
GS120845854028220 [Direct Marking]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2022-08-30
Device Publish Date2021-05-30

On-Brand Devices [GENESYS CROSSFT]

308458540424835.5MM GENESYS CROSSFT SUTURE ANCHOR WITH THREE NO. 2 (5 METRIC) HI-FI SUTURES
20845854042721GENESYS CROSSFT 6.5MM SUTURE ANCHOR, W/ 3 HI-FI NO. 2 (5 METRIC) SUTURES W/ NEEDLES
20845854042714GENESYS CROSSFT 6.5MM SUTURE ANCHOR, W/ 2 HI-FI NO. 2 (5 METRIC) SUTURES W/ NEEDLES
20845854042707GENESYS CROSSFT 5.5MM SUTURE ANCHOR, W/ 3 HI-FI NO. 2 (5 METRIC) SUTURES W/ NEEDLES
20845854042691GENESYS CROSSFT 5.5MM SUTURE ANCHOR, W/ 2 HI-FI NO. 2 (5 METRIC) SUTURES W/ NEEDLES
20845854042684GENESYS CROSSFT 4.5MM SUTURE ANCHOR, W/ 3 HI-FI NO. 2 (5 METRIC) SUTURES W/ NEEDLES
20845854042677GENESYS CROSSFT 4.5MM SUTURE ANCHOR, W/ 2 HI-FI NO. 2 (5 METRIC) SUTURES W/ NEEDLES
208458540425096.5MM GENESYS CROSSFT SUTURE ANCHOR WITH THREE NO. 2 (5 METRIC) HI-FI SUTURES
208458540424936.5MM GENESYS CROSSFT SUTURE ANCHOR WITH TWO NO. 2 (5 METRIC) HI-FI SUTURES
208458540424795.5MM GENESYS CROSSFT SUTURE ANCHOR WITH TWO NO. 2 (5 METRIC) HI-FI SUTURES
208458540424624.5MM GENESYS CROSSFT SUTURE ANCHOR WITH THREE NO. 2 (5 METRIC) HI-FI SUTURES
20845854042455GENESYS CROSSFT 4.5MM SUTURE ANCHOR, WITH TWO #2 (5METRIC) HI-FI SUTURES
20845854034597GENESYS CROSSFT 5.5MM SUTURE ANCHOR, W/ 2 HI-FI NO. 2 (5 METRIC) SUTURES W/ NEEDLES
20845854034580GENESYS CROSSFT 4.5MM SUTURE ANCHOR, W/ 3 HI-FI NO. 2 (5 METRIC) SUTURES W/ NEEDLES
20845854034573GENESYS CROSSFT 4.5MM SUTURE ANCHOR, W/ 2 HI-FI NO. 2 (5 METRIC) SUTURES W/ NEEDLES
208458540345664.5MM GENESYS CROSSFT SUTURE ANCHOR WITH TWO NO. 2 (5 METRIC) HI-FI SUTURES
208458540267835.5MM GENESYS CROSSFT SUTURE ANCHOR WITH TWO NO. 2 (5 METRIC) HI-FI SUTURES
208458540267764.5MM GENESYS CROSSFT SUTURE ANCHOR WITH THREE NO. 2 (5 METRIC) HI-FI SUTURES
10845854032664GENESYS CROSSFT TAP, 6.5MM
10845854032640GENESYS CROSSFT TAP, 5.5MM
10845854032626GENESYS CROSSFT TAP, 4.5MM
10845854034620GENESYS CROSSFT 6.5MM SUTURE ANCHOR, W/ 3 HI-FI #2 (5 METRIC) SUTURES W/NEEDLES
10845854028223GENESYS CROSSFT PUNCH, 5.5MM
10845854034613GENESYS CROSSFT 6.5MM SUTURE ANCHOR, W/ 2 HI-FI (5 METRIC) SUTURES W/NEEDLES
10845854034606GENESYS CROSSFT 5.5MM SUTURES ANCHOR, W/ 3 HI-FI #2 (5 METRIC) SUTURES W/NEEDLES
108458540268166.5MM CROSSFT-BC ANCHOR, W/DISP, TRP
108458540268096.5MM CROSSFT-BC ANCHOR, W/DISP, DBL
108458540267935.5MM CROSSFT-BC ANCHOR, W/DISP, TRP

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.