URIVerse™

FDA UDI

Class I (US FDA UDI)

by Copan Wasp Srl

Identity

Trade Name: URIVerse™ FDA UDI
Generic Name: Pipetting system IVD FDA UDI
Device Name: URIVerse™ FDA UDI
Model / Reference: W095 FDA UDI
Description: URIVerse™ FDA UDI

Identifiers

Catalog Number: W095 FDA UDI
Primary DI / UDI-DI: 58059796361700 FDA UDI
FDA Product Code: JQW FDA UDI
GMDN Term: Pipetting system IVD FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 862.2750 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pipetting system IVD

URIVerse™ by Copan Wasp Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Copan Wasp Srl

Sources (1)

FDA UDI dcf579f0-4c10-4482-bec2-fd798e59a934 35 fields · synced Jun 8, 2026