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Gemcore360

FDA UDI

Class I (US FDA UDI)

by Advanced Medical Solutions Limited

Identity

Trade Name
GEMCORE360 FDA UDI
Generic Name
Exudate-absorbent dressing, non-gel, non-antimicrobial FDA UDI
Device Name
Silicone Trilaminate Foam Border FDA UDI
Model / Reference
Silicone Foam Adhesive Border FDA UDI
Description
Silicone Trilaminate Foam Border FDA UDI

Identifiers

Catalog Number
AM-WC-SFB44 FDA UDI
Primary DI / UDI-DI
10610888000213 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Exudate-absorbent dressing, non-gel, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4020 FDA UDI
Commercial Distribution
Not 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Gemcore360 by Advanced Medical Solutions Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 23520850-3b6b-4124-8735-5e111f4eb89f 35 fields · synced Jun 8, 2026