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UriFree

FDA UDI

Class I (US FDA UDI)

by Copan Italia Spa

Identity

Trade Name
UriFree FDA UDI
Generic Name
Specimen transfer scooping tool IVD FDA UDI
Device Name
Sterile container for urine transfer FDA UDI
Model / Reference
2E127S50.A FDA UDI
Description
Sterile container for urine transfer FDA UDI

Identifiers

Catalog Number
2E127S50.A FDA UDI
Primary DI / UDI-DI
38053326010966 FDA UDI
FDA Product Code
KDT FDA UDI
GMDN Term
Specimen transfer scooping tool IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 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

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

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: Specimen transfer scooping tool IVD

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

Similar devices

Also classified as Specimen transfer scooping tool IVD.

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 defc610e-3ef3-49e5-8413-cd3b99199344 34 fields · synced Jun 1, 2026