Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

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

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

E3897 Micro Serrefine — Class I MDR by Bausch & Lomb GmbH

MD Atlas
Bausch & Lomb GmbH

EUDAMED last updated this device on Mar 10, 2026

E3897 Micro Serrefine

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: 04058935011413
Reference / catalog number: E3897

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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: E3897 Micro Serrefine
UDI-DI code: 04058935011413
Basic UDI-DI: 4058935-000000-AC
Reference / catalog number: E3897
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

Related devices

Aspirating Cannula HandpieceB-04058935009304On the market I/A Handpiece, Angled 20°B-04058935009281On the market I/A Handpiece, Angled 90°B-04058935009298On the market I/A Handpiece, StraightB-04058935009212On the market 16/22GA I/A Handpiece, Angled 60°B-04058935009250On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.