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

2008 — Class I MDR by Maneped GmbH

MD Atlas
Maneped GmbH

EUDAMED last updated this device on May 18, 2026

2008

42505503-Nagelzangen-87

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Maneped GmbH
UDI-DI code: 04250550300150
Reference / catalog number: 2008

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: Maneped GmbH
SRN: DE-MF-000053625
Manufacturer status: Active

Related devices

Excellent Hautzange 10 cm, Schneide 3.5 mm - Doppelfeder42505503-Hautzangen-V2On the market 700242505503-Hautzangen-V2On the market 600142505503-Hautzangen-V2On the market 700342505503-Hautzangen-V2On the market 600242505503-Hautzangen-V2On 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.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04250550300150
Basic UDI-DI: 42505503-Nagelzangen-87
Reference / catalog number: 2008
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: 13 MU10

EMDN nomenclature code(s)

L031399GENERAL SURGERY FORCEPS, REUSABLE - 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