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

dOFM Perfusate Bag 10ml — Class IIa MDR by JOANNEUM RESEARCH…

MD Atlas
JOANNEUM RESEARCH Forschungsgesellschaft mbH

EUDAMED last updated this device on Jul 17, 2024

dOFM Perfusate Bag 10ml

912012209PEBBR

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: JOANNEUM RESEARCH Forschungsgesellschaft mbH
UDI-DI code: 09120122090060
Reference / catalog number: PEB001

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: JOANNEUM RESEARCH Forschungsgesellschaft mbH
SRN: AT-MF-000017155
Manufacturer status: Active

Market distribution

Primary placement in Austria; available across 2 countries total.

Country	On market since	Until
AustriaPrimary placement	Mar 1, 2023	Still on market
Germany	Mar 1, 2023	Still on market

Device identification

Trade name: dOFM Perfusate Bag 10ml
UDI-DI code: 09120122090060
Basic UDI-DI: 912012209PEBBR
Reference / catalog number: PEB001
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: Perfusate bag to perform openflow microperfusion
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A99DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - 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

dOFM Dermal Catheter912012209DEA9TOn the market dOFM Linear Probe Connector912012209LPCC8On the market dOFM Pull Tubing ECO 3-Channel912012209PLLD2On the market dOFM Pull Tubing ECO 4-Channel912012209PLLD2On the market dOFM Pull Tubing Low Bind 3-Channel912012209PLLD2On 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.