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Bausch + Lomb

FDA UDI

Class II (US FDA UDI)

by Bausch & Lomb Incorporated

Identity

Trade Name
Bausch + Lomb FDA UDI
Generic Name
Faecal-incontinence vaginal insert sizer FDA UDI
Device Name
HANDPIECE BI-MANUAL ASP 19GA FDA UDI
Model / Reference
MVS1083 FDA UDI
Description
HANDPIECE BI-MANUAL ASP 19GA FDA UDI

Identifiers

Catalog Number
MVS1083 FDA UDI
Primary DI / UDI-DI
00757770472222 FDA UDI
FDA Product Code
HQC FDA UDI
GMDN Term
Faecal-incontinence vaginal insert sizer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4670 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Faecal-incontinence vaginal insert sizer

Bausch + Lomb by Bausch & Lomb Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Faecal-incontinence vaginal insert sizer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bausch & Lomb Incorporated

Sources (1)

  • FDA UDI 6aee56b1-62b2-400d-8d9f-4a5c0c80201d 34 fields · synced Jun 8, 2026