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AllCare

FDA UDI

Class I (US FDA UDI)

by Allcare, Inc.

Identity

Trade Name
AllCare FDA UDI
Generic Name
Dissection sponge FDA UDI
Device Name
TONSIL SPONGES, 1", 5/PK, X-RAY DETECTABLE, COTTON, STERILE FDA UDI
Model / Reference
STS-5M FDA UDI
Description
TONSIL SPONGES, 1", 5/PK, X-RAY DETECTABLE, COTTON, STERILE FDA UDI

Identifiers

Catalog Number
STS-5M FDA UDI
Primary DI / UDI-DI
00182921000960 FDA UDI
FDA Product Code
GDI FDA UDI
GMDN Term
Dissection sponge FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

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: Dissection sponge

AllCare by Allcare, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dissection sponge.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Allcare, Inc.

Sources (1)

  • FDA UDI 9763437b-8343-467c-a9fb-6c0a4623adcd 36 fields · synced Jun 6, 2026