35-40-205

Organization name

VBM Medizintechnik GmbH

SRN

DE-MF-000005907

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

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

• CW999

  Contra-indications: In non-fasted patient with increased risk of aspiration, mask ventilation must not be employed except in emergency situations.

Primary placement in Germany; available across 32 countries total.

Trade name

not provided

UDI-DI code

04250105600025

Basic UDI-DI

42501056-1.5.1-VK

Reference / catalog number

35-40-205

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

https://ifu.vbm-medical.de/

Clinical sizes

• #5

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• R03010101ANAESTHETIC FACE MASKS