Arthrex®

FDA UDI

Class I (US FDA UDI)

by Arthrex, Inc.

Identity

Trade Name: Arthrex® FDA UDI
Generic Name: Orthopaedic operating table top FDA UDI
Device Name: Weight Hanger, 10lb (4.5kg), S3 FDA UDI
Model / Reference: AR-1650-04 FDA UDI
Description: Weight Hanger, 10lb (4.5kg), S3 FDA UDI

Identifiers

Catalog Number: AR-1650-04 FDA UDI
Primary DI / UDI-DI: 00888867245075 FDA UDI
FDA Product Code: FMP FDA UDI
GMDN Term: Orthopaedic operating table top FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.6450 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Orthopaedic operating table top

Arthrex® by Arthrex, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic operating table top.

ISI — INSTRUMENT SPECIALISTS, INC. · Class I
Carter — INSTRUMENT SPECIALISTS, INC. · Class I
ISI — INSTRUMENT SPECIALISTS, INC. · Class I
Carter — INSTRUMENT SPECIALISTS, INC. · Class I
C-Thru — INSTRUMENT SPECIALISTS, INC. · Class I
Carter — INSTRUMENT SPECIALISTS, INC. · Class I
C-Thru — INSTRUMENT SPECIALISTS, INC. · Class I
ISI — INSTRUMENT SPECIALISTS, INC. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Arthrex, Inc.

Sources (1)

FDA UDI 2dc3990d-468c-4432-98eb-71378c1928d8 35 fields · synced May 30, 2026