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

314S — Class I MDR by Bernhard Hermle GmbH

MD Atlas
Bernhard Hermle GmbH

EUDAMED last updated this device on Feb 6, 2026

314S

426072582I5-SondeLakrimT7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Bernhard Hermle GmbH
UDI-DI code: 04260725822721
Reference / catalog number: 314S

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: Bernhard Hermle GmbH
SRN: DE-MF-000010226
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 04260725822721
Basic UDI-DI: 426072582I5-SondeLakrimT7
Reference / catalog number: 314S
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: Sonde BOWMAN, Stahl, geknöpft, 0000/000, 130mm lang
Additional information URL: https://www.hermle-medizintechnik.de/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L1705OPHTHALMOLOGY PROBES, REUSABLE

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

1762426072582Ir-SpatelAuge7KOn the market 970426072582I1-NierenschalTGOn the market 251426072582Ir-ChirLoeffelG9On the market 975426072582I1-ZangeKornEBOn the market 357-2426072582I5-KanueleAugLKMOn 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.