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Holloware Instruments

by Mehrish Industries

Ref M22000HI

Holloware Instruments (M22000HI) is a Class I device made by Mehrish Industries, registered in EUDAMED on 27 Jun 2026 (Basic UDI-DI ++G410M22000HITT), active as of 7 Nov 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++G410M22000HITT Basic UDI-DI Date27 Jun 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
M22000HI
Primary DI / UDI-DI
+G410M22000HITT, +G410HOLLOWAREINSTRUZ4
Basic UDI-DI
++G410M22000HITT, ++G410HOLLOWAREINSTRUZ4
EMDN code
V0402 Clinical use trays and bowls
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
PK-MF-000031501
Authorised representative
ANTEX MEDI SOLUTION DE-AR-000008078

Similar devices in this category

Other devices filed under CLINICAL USE TRAYS AND BOWLS.

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Properties

  • Sterilise before use
  • Reusable
Other properties (12, all answered No)