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MicroBlate Flex

by Creo Medical 3 variants

Ref 7-AB1-003

MicroBlate Flex (7-AB1-003) is a medical device (EU MDR Class IIb; EMDN category electrosurgery devices) made by Creo Medical, registered in EUDAMED on 3 Apr 2025 (Basic UDI-DI 506035956MICROBLATEAB13Z), active as of 22 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506035956MICROBLATEAB13Z Basic UDI-DI 05060359560988UDI-DIDate3 Apr 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
AB1 Electrosurgical Instrument
Model / reference
7-AB1-003
Primary DI / UDI-DI
05060359560988
Basic UDI-DI
506035956MICROBLATEAB13Z
EMDN code
K0299 Electrosurgery devices, single-use - other
Device class
Class IIb
EU registration type
Standard device
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
GB-MF-000019076
Authorised representative
Creo Medical, S.L.U. ES-AR-000001355

Similar devices in this category

Other devices filed under ELECTROSURGERY DEVICES, SINGLE-USE - OTHER.

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See all devices from Creo Medical →

Properties

  • Supplied sterile
Other properties (13, all answered No)