Skip to content

CT/MR M.A.C. Interstitial GYN Template, 1.65mmBebig 1506-1.65

by Mick Radio Nuclear Instrument, Inc

Ref 1506-1.65

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

CE MDD

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/MDD EUDAMED NumberB-00817330024183 Basic UDI-DI 00817330024183UDI-DIDate21 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00817330024183 UDI-DI Date26 Sep 2016ListedStatusListed 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  • Withdrawn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/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
CT/MR M.A.C. Interstitial GYN Template,1.65mm Bebig EUDAMED
CT/MR M.A.C. Interstitial GYN Template,1.65mmBebig GUDID
Generic Name
General-purpose brachytherapy system applicator, manual
Device Name
CT/MR M.A.C. Interstitial GYN Template Bebig
Model / Ref / Catalog
1506-1.65
Primary DI / UDI-DI
00817330024183
Basic UDI-DI
B-00817330024183
FDA Product Code
JAQ
EMDN Code
Z11010380 Brachytherapy radiation systems - hardware accessories
GMDN Term
General-purpose brachytherapy system applicator, manual
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
892.5700
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
MRI Safety
MR Safe

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class II

Other devices from Mick Radio-Nuclear Instruments, Inc.

See all devices from Mick Radio-Nuclear Instruments, Inc. →

Properties

  • Serial Number
  • Manufacturing Date

Other properties (20)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No