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Urocap IV Light

FDA UDI

Class II (US FDA UDI)

by Laborie Medical Technologies Canada ULC

Identity

Trade Name
Urocap IV Light FDA UDI
Generic Name
Urine flowmeter, reusable FDA UDI
Model / Reference
UCL1000 FDA UDI

Identifiers

Primary DI / UDI-DI
10627825005958 FDA UDI
FDA Product Code
EXY FDA UDI
GMDN Term
Urine flowmeter, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Urine flowmeter, reusable

Urocap IV Light by Laborie Medical Technologies Canada ULC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urine flowmeter, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 319328c6-25e5-4c48-bc0a-64f29d73d5dc 32 fields · synced May 30, 2026