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Ubc

FDA UDI

Class I (US FDA UDI)

by Andover Healthcare Inc.

Identity

Trade Name
UBC FDA UDI
Generic Name
Compression bandaging kit FDA UDI
Device Name
Unna Boot Calamine A single roll of soft foam impregnated with calamine. NL W/IND TN/PK 3" FDA UDI
Model / Reference
NL W/IND TN/PK 3" FDA UDI
Description
Unna Boot Calamine A single roll of soft foam impregnated with calamine. NL W/IND TN/PK 3" FDA UDI

Identifiers

Catalog Number
8830UBC-TN FDA UDI
Primary DI / UDI-DI
10724004611815 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Compression bandaging kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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

No

FDA UDI

Convenience Kit

Yes

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: Compression bandaging kit

Ubc by Andover Healthcare Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Compression bandaging kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Andover Healthcare Inc.

Sources (1)

  • FDA UDI 631cc604-3d1a-4154-b584-f2cd7d553e36 35 fields · synced May 30, 2026