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

2042-LMU-XS — Class I MDR by Puhla Oy

MD Atlas
Puhla Oy

EUDAMED last updated this device on Sep 25, 2024

2042-LMU-XS

643007415phlwearhygKP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Puhla Oy
UDI-DI code: 06430074151225
Reference / catalog number: 2042-LMU-XS

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: Puhla Oy
SRN: FI-MF-000042691
Manufacturer status: Inactive

Market distribution

Primary placement in Finland; available across 1 country total.

Placed on the market in Finland; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 06430074151225
Basic UDI-DI: 643007415phlwearhygKP
Reference / catalog number: 2042-LMU-XS
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: Hygieniahaalari pitkällä polveen asti avautuvalla vetoketjulla, luumun värinen, koko XS.
Additional information URL: https://www.puhla.com/tuote/hygieniahaalari-luumu/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T0299PROTECTION DRAPES AND GARMENTS - 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

2041-HRM-XL643007415phlwearhygKPOn the market 2041-HRM-M643007415phlwearhygKPOn the market 2041-HRM-XS643007415phlwearhygKPOn the market 2041-HRM-L643007415phlwearhygKPOn the market 2041-HRM-S643007415phlwearhygKPOn 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.