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Conmed

FDA UDI

Class I (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CONMED FDA UDI
Generic Name
Ligament graft sizer, noninvasive FDA UDI
Device Name
Graft Sizing Ring, Large FDA UDI
Model / Reference
GFT-LG FDA UDI
Description
Graft Sizing Ring, Large FDA UDI

Identifiers

Catalog Number
GFT-LG FDA UDI
Primary DI / UDI-DI
10845854042380 FDA UDI
FDA Product Code
HWT FDA UDI
GMDN Term
Ligament graft sizer, noninvasive FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ligament graft sizer, noninvasive

Conmed by Conmed Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ligament graft sizer, noninvasive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 9c76aa3d-3d54-45af-859c-38c81c6cb661 36 fields · synced May 30, 2026