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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Eye Speculum — 2 UDI-DI variants, MDR (Bausch & Lomb GmbH)

MD Atlas
Bausch & Lomb GmbH

Data from EUDAMED, last updated May 23, 2026

Eye Speculum

4058935-070000-D7

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Bausch & Lomb GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4058935-070000-D7
Device name: Eye Speculum
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: Bausch & Lomb GmbH
SRN: DE-MF-000009142
Country: Germany
Email: DL-HDL-SafetyOff@bausch.com
Phone: +49 6221 823-0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KQCDVWYFZZ55WY73MDEDA3Z1

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Barraquer Lid Speculum24058935005249
Speculum adjustable24058935005263