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Utm®

FDA UDI

Class I (US FDA UDI)

by Copan Italia Spa

Identity

Trade Name
UTM® FDA UDI
Generic Name
General specimen collection kit FDA UDI
Device Name
MINI UTM KIT 3 mL Medium + Regular sterile Flocked Swab FDA UDI
Model / Reference
355C FDA UDI
Description
MINI UTM KIT 3 mL Medium + Regular sterile Flocked Swab FDA UDI

Identifiers

Catalog Number
355C FDA UDI
Primary DI / UDI-DI
28053326001431 FDA UDI
FDA Product Code
JSM FDA UDI
GMDN Term
General specimen collection kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2390 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

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

No

FDA UDI

Category: General specimen collection kit

Utm® by Copan Italia Spa — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General specimen collection kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Copan Italia Spa

Sources (1)

  • FDA UDI 01533841-764c-4f69-9d5e-5dd569777ca4 34 fields · synced Jun 1, 2026