15.7001

GUDID 20845854024222

STANDARD GRASPER STRAIGHT, 2MM 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 ID20845854024222
NIH Device Record Keyb5926a13-063c-482c-9354-de0173a13502
Commercial Distribution StatusIn Commercial Distribution
Version Model Number15.7001
Catalog Number15.7001
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 Millimeter
Length90 Millimeter
Width2 Millimeter
Length90 Millimeter
Width2 Millimeter
Length90 Millimeter
Width2 Millimeter
Length90 Millimeter
Width2 Millimeter
Length90 Millimeter
Width2 Millimeter
Length90 Millimeter
Width2 Millimeter
Length90 Millimeter
Width2 Millimeter
Length90 Millimeter
Width2 Millimeter
Length90 Millimeter
Width2 Millimeter
Length90 Millimeter
Width2 Millimeter
Length90 Millimeter
Width2 Millimeter
Length90 Millimeter
Width2 Millimeter
Length90 Millimeter
Width2 Millimeter
Length90 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS110845854024225 [Primary]
GS120845854024222 [Direct Marking]

FDA Product Code

GENFORCEPS, GENERAL & PLASTIC SURGERY

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[20845854024222]

Moist Heat or Steam Sterilization

[20845854024222]

Moist Heat or Steam Sterilization

[20845854024222]

Moist Heat or Steam Sterilization

[20845854024222]

Moist Heat or Steam Sterilization

[20845854024222]

Moist Heat or Steam Sterilization

[20845854024222]

Moist Heat or Steam Sterilization

[20845854024222]

Moist Heat or Steam Sterilization

[20845854024222]

Moist Heat or Steam Sterilization

[20845854024222]

Moist Heat or Steam Sterilization

[20845854024222]

Moist Heat or Steam Sterilization

[20845854024222]

Moist Heat or Steam Sterilization

[20845854024222]

Moist Heat or Steam Sterilization

[20845854024222]

Moist Heat or Steam Sterilization

[20845854024222]

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

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10845854026809 - GENESYS CROSSFT2024-04-18 6.5MM CROSSFT-BC ANCHOR, W/DISP, DBL
10845854026816 - GENESYS CROSSFT2024-04-18 6.5MM CROSSFT-BC ANCHOR, W/DISP, TRP
10845854027868 - GENESYS PRESSFT2024-04-18 GENESYS PRESS FT 2.1 W/ONE # 2 (5 METRIC) HI-FI SUTURE, HIP
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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