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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

23002 — Class I MDR by Mills Enterprises LTD Oy

MD Atlas
Mills Enterprises LTD Oy

EUDAMED last updated this device on Dec 20, 2023

23002

642061171L1995SZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Mills Enterprises LTD Oy
UDI-DI code: 06420611710220
Reference / catalog number: 23002

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Manufacturer information

Organization name: Mills Enterprises LTD Oy
SRN: FI-MF-000010101
Manufacturer status: Active

Related devices

Mills Lambswool 100 g642061171L1995SZOn the market Mills Lambswool 100 g642061171L1995SZOn the market Mills Lambswool 20 g642061171L1995SZOn the market Mills Lambswool 20 g642061171L1995SZOn the market Mills Lambswool 20 g642061171L1995SZOn the market

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.

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: 06420611710220
Basic UDI-DI: 642061171L1995SZ
Reference / catalog number: 23002
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: MILLS LAMPAANVILLA MILLS LAMMULL MILLS LAMBSWOOL is 100 % ovine wool, intended for persons who suffer tinea in feet, or other need for protection of the skin against moisture and abrasion. MILLS LAMBSWOOL is intended for treatment and prevent skin abrasion. Lambswool effectively absorbs moisture, and skin remains dry and intact. MILLS LAMBSWOOL is long fiber, soft, specially purified and free of lanoline. May include traces of lanoline. It is intended for single use only and it should be replaced daily. Suitable for hospital and healthcare institutions; to prevent and treatment of foot problems with patients.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M0199WOOL AND SYNTHETIC COTTON - 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

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.