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Tube for Vaginal Sensor, with 3-way Stopcock

FDA UDI

Class II (US FDA UDI)

by Laborie Medical Technologies Canada ULC

Identity

Trade Name
Tube for Vaginal Sensor, with 3-way Stopcock FDA UDI
Generic Name
Perineal orifice incontinence-control electrical stimulation system probe, reusable FDA UDI
Model / Reference
PRB080 FDA UDI

Identifiers

Primary DI / UDI-DI
00627825011044 FDA UDI
FDA Product Code
HIR FDA UDI
GMDN Term
Perineal orifice incontinence-control electrical stimulation system probe, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1425 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Perineal orifice incontinence-control electrical stimulation system probe, reusable

Tube for Vaginal Sensor, with 3-way Stopcock by Laborie Medical Technologies Canada ULC — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Perineal orifice incontinence-control electrical stimulation system probe, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Laborie Medical Technologies Canada ULC

Sources (1)

  • FDA UDI b54e3e25-03d7-4675-aa53-e21d6e09b50d 32 fields · synced May 29, 2026