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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Sterilization container liner FDA UDI
Device Name
WRAP, BONDED,GEMINI,18X18,HVY WT FDA UDI
Model / Reference
GEM4118S FDA UDI
Description
WRAP, BONDED,GEMINI,18X18,HVY WT FDA UDI

Identifiers

Catalog Number
GEM4118S FDA UDI
Primary DI / UDI-DI
10080196184989 FDA UDI
FDA Product Code
FRG FDA UDI
GMDN Term
Sterilization container liner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Sterilization container liner

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

Similar devices

Also classified as Sterilization container liner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 78eeb71e-ae2c-447b-a295-5c49f3355297 35 fields · synced Jun 8, 2026