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Anovator M1

by Wuhan Zhaike Network Technology Company, Limited

Ref M1Model M0 M1 M2 M3 M4 M5 M6 M7 M8 M9 K0 K1 K2 K3 K4 K5 K6 K7 K8 K9 A0 A1 A2 A3 A4 A5 A6 A7 A8 A9 S0 S1 S2 S3 S4 S5 S6 S7 S8 S9 T0 T1 T2 T3 T4 T5 T6 T7 T8 T9

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number697703552M1ZE Basic UDI-DI 16977035520111UDI-DIDate16 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number16977035520111 UDI-DI Date27 Mar 2026ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Body Composition Analyzer EUDAMED
Anovator GUDID
Generic Name
Bioelectrical body composition analyser
Model / Reference
M1, M0 M1 M2 M3 M4 M5 M6 M7 M8 M9 K0 K1 K2 K3 K4 K5 K6 K7 K8 K9 A0 A1 A2 A3 A4 A5 A6 A7 A8 A9 S0 S1 S2 S3 S4 S5 S6 S7 S8 S9 T0 T1 T2 T3 T4 T5 T6 T7 T8 T9
Primary DI / UDI-DI
16977035520111
Basic UDI-DI
697703552M1ZE
Direct Marketing DI
16977035520111
FDA Product Code
PUH
EMDN Code
Z12099001 Body impedance analysers
GMDN Term
Bioelectrical body composition analyser
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
870.2770
EU market of registration
Austria
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class II

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Properties

  • Measuring Function
  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (18)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No