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coflex® Extractor pliers

by Paradigm Spine GmbH

Ref UAT40450, UAC00000, UBT10014, UAT10300, UCT00010, UCT00012, URT00008, UDT10007, UAT10010, UAT40201, UXT10010, UAT00010, UAT00008, UET00010, UBT10010, UCT00014, UDT00007, UAT00014, UET00014, UBT10012, UCT00016, UAT10016, UET00016, UET00012

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

CE MDR CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 25 Oct 2026

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/MDD EUDAMED Number0426014889001-009WL Basic UDI-DI Date16 Feb 2026RegisteredStatusActive
European UnionCE/MDR EUDAMED Number0426014889001-009WL Basic UDI-DI Date16 Feb 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04260148898600 UDI-DI Date29 Jun 2017ListedStatusListed 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.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 25 Oct 2026.

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade Name
coflex® Extractor pliers EUDAMED
coflex® EUDAMED
coflex Trial with wings, 10mm GUDID
coflex Trial, 10mm GUDID
coflex Revision pliers GUDID
coflex Trial with wings and window, Size 14 GUDID
coflex Trial with wings, 16mm GUDID
coflex Trial with wings, 12mm GUDID
coflex Trial with wings and window, Size 10 GUDID
coflex extractor pliers GUDID
coflex wing loosener GUDID
coflex Trial, 12mm GUDID
coflex Trial with wings and window, Size 8 GUDID
coflex Trial with upper wings GUDID
coflex Trial with wings, 14mm GUDID
coflex Trial with wings and window, Size 12 GUDID
coflex Trial with wings and window, Size 16 GUDID
coflex Trial with lower wings GUDID
coflex trial with guide and x-ray marker, 10mm GUDID
coflex Trial, 14mm GUDID
Generic Name
Orthopaedic prosthesis implantation positioning instrument, reusable
Device Name
coflex® Sterilization tray
coflex® trial, 14mm
coflex® Revision pliers
coflex® Trial with wings, 10mm
coflex® Trial with wings, 12mm
coflex® Trial with wings and window, Size 8
coflex® Trial with lower wings
coflex® Trial, 10mm
coflex® Wing loosener
coflex® Trial with guide and x-ray marker, 8mm
coflex®™ Trial, 8mm
coflex® Trial with wings and window, Size 10
coflex® Trial with wings, 14mm
coflex® Trial with upper wings
coflex® Trial with wings and window, Size 14
coflex® Trial, 12mm
coflex® Trial with wings, 16mm
coflex®Trial, 16mm
coflex® Trial with wings and window, Size 16
coflex® Trial with wings and window, Size 12
coflex® Trial with wings, 8mm
Model / Reference
UAT40450, UAC00000, UCT00010, UBT10010, UAT10300, UET00014, UCT00016, UCT00012, UET00010, UAT40201, UBT10012, UDT00007, UCT00014, UET00012, UET00016, UDT10007, UXT10010, UBT10014, URT00008, UAT10010, UAT00010, UAT00008, UAT00014, UAT10016, UET00008
Primary DI / UDI-DI
04260148898600, 04260148890154, 04260148898815, 04260148898716, 04260148899003, 04260148898907, 04260148898846, 04260148898822, 04260148898884, 04260148897832, 04260148898723, 04260148898877, 04260148898853, 04260148898839, 04260148898891, 04260148898914, 04260148898860, 04260148897757, 04260148898730, 04260148898662, 04260148890079, 04260148890062, 04260148890093, 04260148898693
Basic UDI-DI
0426014889001-009WL, 0426014889001-001W4, B-04260148898730, 0426014889001-007WG, B-04260148898815, B-04260148898822, B-04260148898877, B-04260148898860, B-04260148898662, 0426014889001-008WJ, B-04260148897757, B-04260148890079, B-04260148890062, B-04260148898884, B-04260148898716, B-04260148898839, B-04260148898853, B-04260148890093, B-04260148898907, B-04260148898723, B-04260148898846, B-04260148898693, B-04260148898914, B-04260148898891, 0426014889018-0137, 0426014889018-0239
Direct Marketing DI
04260148898600
04260148890154
04260148899003
04260148897832
04260148898723
04260148898815
04260148898846
04260148890079
04260148898891
04260148898907
04260148898853
04260148898822
04260148898839
PMA Number
FDA Product Code
NQO
EMDN Code
L091101, S010399, L091199
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, reusable
Device Class
Class I EUDAMED
Class IIa EUDAMED
Class III GUDID
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class I
Class IIa
GUDID
Class III

Manufacturer details

EUDAMED SRN
DE-MF-000011231

Other devices from Paradigm Spine GmbH

See all devices from Paradigm Spine GmbH →

Properties

  • Reusable YesEUDAMEDNoEUDAMED
  • Prescription Use
  • Lot / Batch Number

Other properties (21)

  • Sterile: No
  • Single Use: No
  • Implantable: 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
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No