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

IFA — IVDR Class A IVDR by Eifelfango Chem. Pharm.…

MD Atlas
Eifelfango Chem. Pharm. Werk GmbH & Co. KG

EUDAMED last updated this device on Jan 29, 2026

IFA

PP07140NATRI07

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Eifelfango Chem. Pharm. Werk GmbH & Co. KG
UDI-DI code: 110076215874
Reference / catalog number: IFA

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: Eifelfango Chem. Pharm. Werk GmbH & Co. KG
SRN: DE-MF-000009424
Manufacturer status: Active

Related devices

IFAPP07140FANGO09On the market IFAPP07140FANGO09On the market IFAPP07140NATRI07On the market IFAPP07140NATRI07On the market IFAPP07140NATRI07On 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: not provided
UDI-DI code: 110076215874
Basic UDI-DI: PP07140NATRI07
Reference / catalog number: IFA
Issuing entity: IFA

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Erythrocyte Sedimentation Rate Test
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W01030107ERYTHROCYTE SEDIMENTATION RATE (ESR) TEST

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification