Skip to content

Maam

by Tex Acces MCV S.R.L. 1,000+ variants

Part of a family of 307 devices: see the family page

Ref MLP 03 130 M

Maam (MLP 03 130 M) is a Class I device made by Tex Acces MCV S.R.L., registered in EUDAMED on 11 May 2026 (Basic UDI-DI 59447591COS6D), active as of 23 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number59447591COS6D Basic UDI-DI 05944759120150UDI-DIDate11 May 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Postoperative compressive bodysuits
Model / reference
MLP 03 130 M
Primary DI / UDI-DI
05944759120150
Basic UDI-DI
59447591COS6D
EMDN code
M030499 Elastic bandages, support and compression - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Romania

Manufacturer details

EUDAMED SRN
RO-MF-000029775

Related devices

Category: Compression/pressure sock/stocking, reusable

Similar devices in this category

Other devices filed under ELASTIC BANDAGES, SUPPORT AND COMPRESSION.

Other devices from Tex Acces MCV S.R.L.

  • Maam

    Class I

  • Maam

    Class I

  • Maam

    Class I

  • Maam

    Class I

See all devices from Tex Acces MCV S.R.L. →

Properties

Other properties (14, all answered No)