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Organization name
UDI-DI code
Reference / catalog number

E2160 Cilia Forceps — Class I MDR by Bausch & Lomb GmbH

MD Atlas
Bausch & Lomb GmbH

EUDAMED last updated this device on Mar 10, 2026

E2160 Cilia Forceps

4058935-000000-AC

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Bausch & Lomb GmbH
UDI-DI code: 04058935011321
Reference / catalog number: E2160

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Manufacturer information

Organization name: Bausch & Lomb GmbH
SRN: DE-MF-000009142
Manufacturer status: Active

Market distribution

Primary placement in Netherlands; available across 1 country total.

Placed on the market in Netherlands; per-country availability dates not published.

Device identification

Trade name: E2160 Cilia Forceps
UDI-DI code: 04058935011321
Basic UDI-DI: 4058935-000000-AC
Reference / catalog number: E2160
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L170299OPHTHALMOLOGY FORCEPS, REUSABLE - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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Certificates

Certificate health across this manufacturer's portfolio.

HZ 2520883-1Supplemented
Quality management systemNotified body: 0197Expiry: Apr 26, 2028
HZ 1333770-1Issued
Quality management systemNotified body: 0197Expiry: Apr 26, 2028