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

Nasal Retainer Size 8 — Class I MDR by Batojan

MD Atlas
Batojan

EUDAMED last updated this device on May 7, 2024

Nasal Retainer Size 8

543000296201NRHW

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Batojan
UDI-DI code: 05430002962085
Reference / catalog number: 108

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: Batojan
SRN: BE-MF-000007260
Manufacturer status: Active

Critical warnings

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

CW022
Do not cut connection bridge between both tubes.

Market distribution

Primary placement in Belgium; available across 1 country total.

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

Device identification

Trade name: Nasal Retainer Size 8
UDI-DI code: 05430002962085
Basic UDI-DI: 543000296201NRHW
Reference / catalog number: 108
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: Nostril retainer Size 8
Additional information URL: https://www.pharmacleft.com/
Clinical sizes: 8

EMDN nomenclature code(s)

Q0399ENT DEVICES - 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

101543000296201NRHWOn the market 110543000296201NRHWOn the market 111543000296201NRHWOn the market 102543000296201NRHWOn the market 103543000296201NRHWOn 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.