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Arthrex®

FDA UDI

Class II (US FDA UDI)

by Arthrex, Inc.

Identity

Trade Name
Arthrex® FDA UDI
Generic Name
Surgical staple loading unit, non-cutting FDA UDI
Device Name
SPIKELESS LIGAMENT STAPLE, 6 MM X 20 MM FDA UDI
Model / Reference
AR-1006M FDA UDI
Description
SPIKELESS LIGAMENT STAPLE, 6 MM X 20 MM FDA UDI

Identifiers

Catalog Number
AR-1006M FDA UDI
Primary DI / UDI-DI
00888867002456 FDA UDI
FDA Product Code
JDR FDA UDI
HXJ FDA UDI
GMDN Term
Surgical staple loading unit, non-cutting FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical staple loading unit, non-cutting

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

Similar devices

Also classified as Surgical staple loading unit, non-cutting.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Arthrex, Inc.

Sources (1)

  • FDA UDI adcd2fa4-0ee3-4285-8057-fd74012211e4 35 fields · synced Jun 8, 2026