Organization name
UDI-DI code
Reference / catalog number

Role
Country
Date of registration
Address

Made In Tracker

Legal

About

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

136009-02 — Class IIa MDR by BMV Bender Medical…

MD Atlas
BMV Bender Medical Vertrieb GmbH

Manufacturer information

Organization name: BMV Bender Medical Vertrieb GmbH
SRN: DE-MF-000005283
Manufacturer status: Active

EUDAMED last updated this device on May 14, 2026

136009-02

4251242613-60-01VS

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BMV Bender Medical Vertrieb GmbH
UDI-DI code: 04251242699781
Reference / catalog number: 136009-02

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.

Password

No account yet?

Manufacturer information

Organization name: BMV Bender Medical Vertrieb GmbH
SRN: DE-MF-000005283
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04251242699781
Basic UDI-DI: 4251242613-60-01VS
Reference / catalog number: 136009-02
Issuing entity: GS1

Classification

Risk category: Class IIa
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)

R01058099TRACHEOSTOMY AND LARYNGECTOMY CANNULAS - VARIOUS 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

Manufacturer information

Related devices

136009-02

Manufacturer information

Related devices

Market distribution

Device identification

Classification

Device details

EMDN nomenclature code(s)

Compliance flags

Safety

Substances

Regulatory

Lifecycle

UDI-PI traceability