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

T01020201 — Class I MDR by LABORATOIRES EUROMEDIS

MD Atlas
LABORATOIRES EUROMEDIS

EUDAMED last updated this device on Dec 15, 2023

T01020201

33893612118Z

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LABORATOIRES EUROMEDIS
UDI-DI code: 03389360002082
Reference / catalog number: 107614A

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: LABORATOIRES EUROMEDIS
SRN: FR-MF-000036597
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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: T01020201
UDI-DI code: 03389360002082
Basic UDI-DI: 33893612118Z
Reference / catalog number: 107614A
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: 100
Additional product description: Protéger le patient des risques infectieux, Empêcher les contaminations croisées et les infections, Garantir l’asepsie, Protection physique et chimique de la main
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T01020201VINYL EXAMINATION / TREATMENT GLOVES

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

Casaque chirurgicale standard plus + 2 essuie-mains (Taille L)33893661DCOn the market Casaque chirurgicale standard plus + 2 essuie-mains (Taille XLL)33893661DCOn the market Casaque chirurgicale stérile renforcée + 2 essuie-mains (Taille L) Dimensions : 130±2 X 160±2 cm33893662DEOn the market Casaque chirurgicale stérile renforcée + 2 essuie-mains (Taille XL) Dimensions : 140±2 X 160±2 cm33893662DEOn the market Casaque chirurgicale stérile renforcée + 2 essuie-mains (Taille XLL) Dimensions : 150±2 X 160±2 cm33893662DEOn 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.