2.7009

GUDID 20845854037642

SST FORCEPS, BLUNT, STRAIGHT, 2.75MM X 90MM

Conmed Corporation

Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable
Primary Device ID20845854037642
NIH Device Record Key48fa38df-368c-4290-9c50-7d1132ba4f5c
Commercial Distribution StatusIn Commercial Distribution
Version Model Number2.7009
Catalog Number2.7009
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

Device Dimensions

Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter
Width2.75 Millimeter
Length90 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS110845854037645 [Primary]
GS120845854037642 [Direct Marking]

FDA Product Code

GENFORCEPS, GENERAL & PLASTIC SURGERY

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[20845854037642]

Moist Heat or Steam Sterilization


[20845854037642]

Moist Heat or Steam Sterilization


[20845854037642]

Moist Heat or Steam Sterilization


[20845854037642]

Moist Heat or Steam Sterilization


[20845854037642]

Moist Heat or Steam Sterilization


[20845854037642]

Moist Heat or Steam Sterilization


[20845854037642]

Moist Heat or Steam Sterilization


[20845854037642]

Moist Heat or Steam Sterilization


[20845854037642]

Moist Heat or Steam Sterilization


[20845854037642]

Moist Heat or Steam Sterilization


[20845854037642]

Moist Heat or Steam Sterilization


[20845854037642]

Moist Heat or Steam Sterilization


[20845854037642]

Moist Heat or Steam Sterilization


[20845854037642]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2022-09-16
Device Publish Date2020-09-24

Devices Manufactured by Conmed Corporation

30845854026797 - GENESYS CrossFT, Hi-Fi2024-04-25 5.5 mm GENESYS CrossFT Suture Anchor with Three #2 (5 metric) Hi-Fi Sutures
30845854026803 - GENESYS CrossFT, Hi-Fi2024-04-25 6.5 mm GENESYS CrossFT Suture Anchor with Two #2 (5 metric) Hi-Fi Sutures
30845854026810 - GENESYS CrossFT, Hi-Fi2024-04-25 6.5 mm GENESYS CrossFT Suture Anchor with Three #2 (5 metric) Hi-Fi Sutures
30845854027862 - GENESYS PressFT, Hi-Fi2024-04-25 GENESYS PressFT 2.1 w/One #2 (5 metric) Hi-Fi Suture, HIP (1 White/Black)
30845854027893 - GENESYS PressFT, Hi-Fi2024-04-25 GENESYS PressFT 2.6 w/One #2 (5 metric) Hi-Fi Suture, HIP (1 White/Black)
30845854034600 - GENESYS CrossFT, Hi-Fi2024-04-25 GENESYS CrossFT 5.5 mm Suture Anchor, w/3 Hi-Fi #2 (5 metric) Sutures w/Needles
30845854034617 - GENESYS CrossFT, Hi-Fi2024-04-25 GENESYS CrossFT 6.5 mm Suture Anchor, w/2 Hi-Fi #2 (5 metric) Sutures w/Needles
30653405988643 - Argo Knotless GENESYS2024-04-22 5.5mm Argo Knotless® GENESYSTM Anchor

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