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

HW-005-025 — Class IIa MDR by MTT GmbH

MD Atlas
MTT GmbH

EUDAMED last updated this device on Aug 28, 2024

HW-005-025

426047681TEMPLTPHDRNR

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MTT GmbH
UDI-DI code: 04260476810299
Reference / catalog number: HW-005-025

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: MTT GmbH
SRN: DE-MF-000005849
Manufacturer status: Active

Related devices

HW-001-015426047681MECHARMFUOn the market HW-005-001426047681TEMPLTP1USEFVOn the market HW-005-033 426047681TEMPLTPHDRNROn the market HW-005-030426047681TEMPLTPHDRNROn the market HW-005-027426047681TEMPLTPHDRNROn 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: 04260476810299
Basic UDI-DI: 426047681TEMPLTPHDRNR
Reference / catalog number: HW-005-025
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: 17 MU999
Hole spacing — 3.3 MU50

EMDN nomenclature code(s)

A018002NEEDLE GUIDES

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