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Advanced Shield Max Silver Barrier, 1oz spray

FDA UDI

Class I (US FDA UDI)

by Kericure Inc.

Identity

Trade Name
Advanced Shield Max Silver Barrier, 1oz spray FDA UDI
Generic Name
Skin semi-occlusive dressing, antimicrobial FDA UDI
Device Name
Topical burn and wound dressing, hydrogel barrier antimicrobial with silver,1oz spray FDA UDI
Model / Reference
6051210 FDA UDI
Description
Topical burn and wound dressing, hydrogel barrier antimicrobial with silver,1oz spray FDA UDI

Identifiers

Primary DI / UDI-DI
00858071004171 FDA UDI
FDA Product Code
NAE FDA UDI
GMDN Term
Skin semi-occlusive dressing, antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4022 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

Yes

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Skin semi-occlusive dressing, antimicrobial

Advanced Shield Max Silver Barrier, 1oz spray by Kericure Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin semi-occlusive dressing, antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kericure Inc.

Sources (1)

  • FDA UDI 860060fb-01a3-4a83-9910-84d5b217e192 33 fields · synced Jun 1, 2026