1.12211

GUDID 20845854024154

MICRO SCISSORS, 30 DEG. RIGHT, 3.4MM X 130MM

Conmed Corporation

Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable
Primary Device ID20845854024154
NIH Device Record Key6ca6bfa1-d324-4380-948a-6367a970c766
Commercial Distribution StatusIn Commercial Distribution
Version Model Number1.12211
Catalog Number1.12211
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 Batchfalse
Serial Numbertrue
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

Device Dimensions

Length130 Millimeter
Angle30 degree
Width3.4 Millimeter
Length130 Millimeter
Angle30 degree
Width3.4 Millimeter
Length130 Millimeter
Angle30 degree
Width3.4 Millimeter
Length130 Millimeter
Angle30 degree
Width3.4 Millimeter
Length130 Millimeter
Angle30 degree
Width3.4 Millimeter
Length130 Millimeter
Angle30 degree
Width3.4 Millimeter
Length130 Millimeter
Angle30 degree
Width3.4 Millimeter
Length130 Millimeter
Angle30 degree
Width3.4 Millimeter
Length130 Millimeter
Angle30 degree
Width3.4 Millimeter
Length130 Millimeter
Angle30 degree
Width3.4 Millimeter
Length130 Millimeter
Angle30 degree
Width3.4 Millimeter
Length130 Millimeter
Angle30 degree
Width3.4 Millimeter
Length130 Millimeter
Angle30 degree
Width3.4 Millimeter
Length130 Millimeter
Angle30 degree
Width3.4 Millimeter
Length130 Millimeter
Angle30 degree
Width3.4 Millimeter
Length130 Millimeter
Angle30 degree
Width3.4 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS110845854024157 [Primary]
GS120845854024154 [Direct Marking]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[20845854024154]

Moist Heat or Steam Sterilization

[20845854024154]

Moist Heat or Steam Sterilization

[20845854024154]

Moist Heat or Steam Sterilization

[20845854024154]

Moist Heat or Steam Sterilization

[20845854024154]

Moist Heat or Steam Sterilization

[20845854024154]

Moist Heat or Steam Sterilization

[20845854024154]

Moist Heat or Steam Sterilization

[20845854024154]

Moist Heat or Steam Sterilization

[20845854024154]

Moist Heat or Steam Sterilization

[20845854024154]

Moist Heat or Steam Sterilization

[20845854024154]

Moist Heat or Steam Sterilization

[20845854024154]

Moist Heat or Steam Sterilization

[20845854024154]

Moist Heat or Steam Sterilization

[20845854024154]

Moist Heat or Steam Sterilization

[20845854024154]

Moist Heat or Steam Sterilization

[20845854024154]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2022-09-02
Device Publish Date2020-06-05

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10845854027899 - GENESYS PRESSFT2024-04-18 GENSESYS PRESSFT 2.6 W/ ONE # 2 (5 METRIC) HI-FI- SUTURE, HIP
10845854034606 - GENESYS CROSSFT2024-04-18 GENESYS CROSSFT 5.5MM SUTURES ANCHOR, W/ 3 HI-FI #2 (5 METRIC) SUTURES W/NEEDLES
10845854034613 - GENESYS CROSSFT2024-04-18 GENESYS CROSSFT 6.5MM SUTURE ANCHOR, W/ 2 HI-FI (5 METRIC) SUTURES W/NEEDLES
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