PressFT PCOH

GUDID 10845854901939

PressFT™ Cannulated Obturator, Hip

Conmed Corporation

Rigid endoscope obturator Rigid endoscope obturator Rigid endoscope obturator Rigid endoscope obturator Rigid endoscope obturator Rigid endoscope obturator Rigid endoscope obturator Rigid endoscope obturator Rigid endoscope obturator Rigid endoscope obturator Rigid endoscope obturator Rigid endoscope obturator Rigid endoscope obturator Rigid endoscope obturator
Primary Device ID10845854901939
NIH Device Record Key276a38f7-8fcb-4257-b50f-d811b23204b6
Commercial Distribution Discontinuation2021-05-04
Commercial Distribution StatusNot in Commercial Distribution
Brand NamePressFT
Version Model NumberPCOH
Catalog NumberPCOH
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(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM

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

Device Identifiers

Device Issuing AgencyDevice ID
GS110845854901939 [Primary]

FDA Product Code

NBHAccessories, arthroscopic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10845854901939]

Moist Heat or Steam Sterilization


[10845854901939]

Moist Heat or Steam Sterilization


[10845854901939]

Moist Heat or Steam Sterilization


[10845854901939]

Moist Heat or Steam Sterilization


[10845854901939]

Moist Heat or Steam Sterilization


[10845854901939]

Moist Heat or Steam Sterilization


[10845854901939]

Moist Heat or Steam Sterilization


[10845854901939]

Moist Heat or Steam Sterilization


[10845854901939]

Moist Heat or Steam Sterilization


[10845854901939]

Moist Heat or Steam Sterilization


[10845854901939]

Moist Heat or Steam Sterilization


[10845854901939]

Moist Heat or Steam Sterilization


[10845854901939]

Moist Heat or Steam Sterilization


[10845854901939]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2021-05-04
Device Publish Date2019-08-02

On-Brand Devices [PressFT]

20845854036652PRESSFT 2.6 W/TWO NO. 1 (4 METRIC) HI-FI SUTURES (1 WHITE/GREEN AND 1 WHITE/BLACK)
20845854036645PRESSFT 2.6 W/ ONE NO. 2 (5 METRIC) HI-FI SUTURE, HIP (1 WHITE/BLACK)
20845854036638PRESSFT 2.6 W/ONE NO. 2 (5 METRIC) HI-FI SUTURE (1 WHITE/BLACK)
20845854036621PRESSFT 2.1 W/TWO NO. 0 (3.5 METRIC) HI-FI SUTURES (1 WHITE/BLACK AND 1 WHITE/BLUE)
20845854036614PRESSFT 2.1 W/ ONE NO. 2 (5 METRIC) HI-FI SUTURE, HIP (1 WHITE/BLACK)
20845854036607PRESSFT 2.1 W/ONE NO. 2 (5 METRIC) HI-FI SUTURE (1 WHITE/BLACK)
10845854901922PressFT™ Drill Guide Spike Tip, Hip
10845854901892PressFT™ Drill Guide Crown Tip, Hip
10845854027967PressFT™ Drill Guide, Hip
10845854027912PressFT™ Cannulated Obturator, Hip
20845854600075PressFT™ Flex Drill Bit 2.6 mm, Hip
20845854600068PressFT™ Flex Drill Bit 2.1 mm, Hip
20845854051167PressFT™ Flex 2.6 GENESYS, Hip
20845854051150PressFT™ Flex 2.1 PEEK, Hip
20845854051143PressFT™ Flex 2.1 GENESYS, Hip
20845854051136PressFT™ Flex 2.6 PEEK, Hip
10845854051191PressFT™ Flex Obturator, Hip
10845854051184PressFT™ Flex Curved Drill Guide, Hip
10845854051177PressFT™ Flex Straight Drill Guide, Hip
10845854901915PressFT™ Drill Bit 2.6mm, Hip
10845854901908PressFT™ Drill Bit 2.1mm, Hip
30845854082359PressFT™ Drill Bit 2.1mm, Hip
30845854082342PressFT™ Drill Bit 2.6mm, Hip
30845854082335PressFT™ Drill Guide Spike Tip, Hip
30845854082311PressFT™ Drill Guide Crown Tip, Hip
10845854901939PressFT™ Cannulated Obturator, Hip

Trademark Results [PressFT]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PRESSFT
PRESSFT
88690079 not registered Live/Pending
Conmed Corporation
2019-11-12

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