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Grid Landscape Fiber for PaxScan4336W

by Philips Medical Systems DMC GmbH 2 variants

Ref 989601070821

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0884838BM450SV Basic UDI-DI 00884838087675UDI-DIDate25 Sep 2024RegisteredStatusActive
United StatesGUDID listing GUDID Number00884838087675 UDI-DI Date9 Jan 2023ListedStatusListed 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  • Withdrawn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
Grid Landscape Fiber for PaxScan4336W EUDAMED
Grid Landscape Fiber PaxScan4336W GUDID
Generic Name
Stationary x-ray grid
Device Name
Grid
Model / Reference
989601070821 EUDAMED
9896-010-70821 GUDID
Primary DI / UDI-DI
00884838087675
Basic UDI-DI
0884838BM450SV
FDA Product Code
IXJ
EMDN Code
Z11039080 Various radiodiagnostic and interventional instruments - hardware accessories
GMDN Term
Stationary x-ray grid
Device Class
Class IIb EUDAMED
Class I GUDID
Regulation Number
892.1910
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
989601070821
GUDID
9896-010-70821
Device ClassEUDAMED
Class IIb
GUDID
Class I

Manufacturer details

EUDAMED SRN
DE-MF-000005362

Other devices from Philips Medical Systems DMC GmbH

See all devices from Philips Medical Systems DMC GmbH →

Properties

  • Prescription Use
  • Premarket Exempt
  • Serial Number

Other properties (21)

  • 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
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No