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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
Phacoemulsification/vitrectomy system FDA UDI
Device Name
TSV 23ga Combined Vitrectomy Pack with AFI and Wide Field Illuminator FDA UDI
Model / Reference
BL5523W FDA UDI
Description
TSV 23ga Combined Vitrectomy Pack with AFI and Wide Field Illuminator FDA UDI

Identifiers

Catalog Number
BL5523W FDA UDI
Primary DI / UDI-DI
00757770058174 FDA UDI
FDA Product Code
HQE FDA UDI
GMDN Term
Phacoemulsification/vitrectomy system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4150 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Phacoemulsification/vitrectomy system

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

Similar devices

Also classified as Phacoemulsification/vitrectomy system.

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 e69e2f0f-c974-456b-90b0-5ccabbb29566 34 fields · synced Jun 8, 2026