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Silvrstat

FDA UDI

Class U (US FDA UDI)

by American Biotech Labs

Identity

Trade Name
Silvrstat FDA UDI
Generic Name
Wound hydrogel dressing, antimicrobial FDA UDI
Device Name
Silvrstat Antibacterial Wound Dressing Gel, 3 oz. FDA UDI
Model / Reference
3 oz. FDA UDI
Description
Silvrstat Antibacterial Wound Dressing Gel, 3 oz. FDA UDI

Identifiers

Primary DI / UDI-DI
00831060006639 FDA UDI
510(k) Number
K092826 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Wound hydrogel dressing, antimicrobial FDA UDI

Classification

Device Class
U 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Weight — 85.05 Gram FDA UDI

Category: Wound hydrogel dressing, antimicrobial

Silvrstat by American Biotech Labs — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound hydrogel dressing, antimicrobial.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 47199d27-6c18-4298-af84-00fa4080a7af 36 fields · synced May 30, 2026