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Life Liner

FDA UDI

Class I (US FDA UDI)

by Depuy Orthopaedics, Inc.

Identity

Trade Name
LIFE LINER FDA UDI
Generic Name
Glove liner FDA UDI
Device Name
LIFE LINER STICK & CUT REST GLV RT X-LG FDA UDI
Model / Reference
5200-70-000 FDA UDI
Description
LIFE LINER STICK & CUT REST GLV RT X-LG FDA UDI

Identifiers

Catalog Number
520070000 FDA UDI
Primary DI / UDI-DI
10603295326403 FDA UDI
FDA Product Code
FYE FDA UDI
GMDN Term
Glove liner FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glove liner

Life Liner by Depuy Orthopaedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glove liner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b0f796d4-bcdd-46ac-a783-733d08fe3b17 35 fields · synced Jun 8, 2026