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

Retainer Boscarol OB 1000 (CANNON) — Class I MDR

MD Atlas
Bucher Leichtbau AG

EUDAMED last updated this device on Nov 29, 2022

Retainer Boscarol OB 1000 (CANNON)

7649989816RET-A002PH

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Bucher Leichtbau AG
UDI-DI code: 07649998867191
Reference / catalog number: 1362741

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: Bucher Leichtbau AG
SRN: CH-MF-000017716
Manufacturer status: Active

Related devices

Retainer Corpuls C3 Charged (MIL)7649989816RET-D001Q4On the market 12-2 FOL.STRETCHER7649989816STR-S0033COn the market Adapter dual7649989816SIT-2001P4On the market Adapter Dual (+41)7649989816SIT-2001P4On the market Adapter single7649989816SIT-2001P4On 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.

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: Retainer Boscarol OB 1000 (CANNON)
UDI-DI code: 07649998867191
Basic UDI-DI: 7649989816RET-A002PH
Reference / catalog number: 1362741
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)

V0880MEDICAL SUPPORT EQUIPMENT - ACCESSORIES

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