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

CLAMP FOR MEDICAL RAIL — Class I MDR by LID - SOTRAMET

MD Atlas
LID - SOTRAMET

EUDAMED last updated this device on Jan 23, 2024

CLAMP FOR MEDICAL RAIL

376036183CLAMP8U

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LID - SOTRAMET
UDI-DI code: 03760361830346
Reference / catalog number: ETRPM007

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: LID - SOTRAMET
SRN: FR-MF-000014659
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: CLAMP FOR MEDICAL RAIL
UDI-DI code: 03760361830346
Basic UDI-DI: 376036183CLAMP8U
Reference / catalog number: ETRPM007
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: https://medical.lid-lamps.com/en/mountings-accessories/04-clamp-for-medical-rails/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12010702MOBILE SCIALYTIC LAMPS

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

BELLA376036183BELLA7NOn the market BELLA376036183BELLA7NOn the market BELLA376036183BELLA7NOn the market BELLA376036183BELLA7NOn the market BELLA376036183BELLA7NOn 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.