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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
Medical device service rail clamp FDA UDI
Device Name
Easy Lock Socket, EU FDA UDI
Model / Reference
AR-1627-12EU FDA UDI
Description
Easy Lock Socket, EU FDA UDI

Identifiers

Primary DI / UDI-DI
00615521004439 FDA UDI
FDA Product Code
FWZ FDA UDI
GMDN Term
Medical device service rail clamp 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: Medical device service rail clamp

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

Similar devices

Also classified as Medical device service rail clamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fb43c6fa-53d3-4f29-b063-ac6bf7e4423f 34 fields · synced May 30, 2026