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Bausch + Lomb

FDA UDI

Class I (US FDA UDI)

by Bausch & Lomb Incorporated

Identity

Trade Name
Bausch + Lomb FDA UDI
Generic Name
Lacrimal dilator, reusable FDA UDI
Device Name
PRB LACHRYMAL 5-6 BOWMAN FDA UDI
Model / Reference
E4204 FDA UDI
Description
PRB LACHRYMAL 5-6 BOWMAN FDA UDI

Identifiers

Primary DI / UDI-DI
00757770410248 FDA UDI
FDA Product Code
HNL FDA UDI
GMDN Term
Lacrimal dilator, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

Yes

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: Lacrimal dilator, reusable

For ophthalmic procedures, the PRB LACHRYMAL 5-6 Bowman device from Bausch & Lomb provides a reliable and effective tool for enlarging the lacrimal canal during surgery. This reusable instrument is designed to be used with caution, as it can cause significant irritation or injury if not handled properly.

Similar devices

Also classified as Lacrimal dilator, reusable.

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 8e305794-6942-4762-a1dc-8debddd371c0 33 fields · synced Jul 29, 2026