Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name: Medline FDA UDI
Generic Name: Hand ligament surgical release instrument FDA UDI
Device Name: 010600 @ACUFEX HOOK KNF, STRAIGHT 3.0MM FDA UDI
Model / Reference: 010600R FDA UDI
Description: 010600 @ACUFEX HOOK KNF, STRAIGHT 3.0MM FDA UDI

Identifiers

Catalog Number: 010600R FDA UDI
Primary DI / UDI-DI: 10888277380561 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Hand ligament surgical release instrument FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Hand ligament surgical release instrument

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

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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

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Manufacturer

Manufacturer: Medline Industries, Inc.

Sources (1)

FDA UDI 6ea2cda6-a35b-4298-8834-8d6ac50a9b26 35 fields · synced May 30, 2026