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Arthrex

FDA UDI

Class I (US FDA UDI)

by Allen Medical Systems, Inc.

Identity

Trade Name
Arthrex FDA UDI
Generic Name
Orthopaedic operating table top FDA UDI
Device Name
Clamp for JP OR Bed Clark Rails FDA UDI
Model / Reference
AR-1627-18 FDA UDI
Description
Clamp for JP OR Bed Clark Rails FDA UDI

Identifiers

Primary DI / UDI-DI
00615521004507 FDA UDI
FDA Product Code
FWZ FDA UDI
GMDN Term
Orthopaedic operating table top FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4950 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthopaedic operating table top

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

Similar devices

Also classified as Orthopaedic operating table top.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 07ab07c6-8910-4ed8-819f-36465c0d1775 34 fields · synced May 30, 2026