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

9363 — Class IIa MDD by Oy Fluorplast Ab

MD Atlas
Oy Fluorplast Ab

EUDAMED last updated this device on Apr 21, 2022

9363

B-06430033406632

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Oy Fluorplast Ab
UDI-DI code: 06430033406632
Reference / catalog number: 9363

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: Oy Fluorplast Ab
SRN: FI-MF-000015708
Manufacturer status: Active

Related devices

9360B-06430033406601On the market 9546B-06430033409466On the market 9387B-06430033406878On the market 9462B-06430033404379On the market 9313B-06430033406137On 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 Finland; available across 2 countries total.

Country	On market since	Until
FinlandPrimary placement		Still on market
Sweden		Still on market

Device identification

Trade name: not provided
UDI-DI code: 06430033406632
Basic UDI-DI: B-06430033406632
Reference / catalog number: 9363
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Oxygen Tube
Additional information URL: https://mediman.fi/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

R03010204OXYGEN ADMINISTRATION TUBINGS

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