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Propel

by Conmed Corporation 7 variants

Ref C8944, C8810, C8800, C8948, C8710, C8820, C8945, C8942, C8947, C8620, C8600

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

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 24 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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-20845854015084 Basic UDI-DI Date13 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number20845854015084 UDI-DI Date24 Oct 2015ListedStatusListed 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 24 Oct 2026.

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  • Withdrawn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

Generic Name
Tendon/ligament bone anchor, non-bioabsorbable
Device Name
Orthopedic, Implant, Non-absorbable, Interference Screw, Titanium, Knee, Cannulated
Model / Ref / Catalog
C8944, C8810, C8800, C8948, C8710, C8820, C8945, C8942, C8947, C8620, C8600
Primary DI / UDI-DI
20845854015084, 20845854015220, 20845854014629, 20845854015190, 20845854014612, 20845854014766, 20845854015305, 20845854014636, 20845854015343, 20845854015060, 20845854014834
Basic UDI-DI
B-20845854015084, B-20845854015220, B-20845854014629, B-20845854015190, B-20845854014612, B-20845854014766, B-20845854015305, B-20845854014636, B-20845854015343, B-20845854015060, B-20845854014834
510(k) Number
FDA Product Code
HWC
EMDN Code
P09120605 Interference screws
GMDN Term
Tendon/ligament bone anchor, non-bioabsorbable
Device Class
Class IIb EUDAMED
Class II GUDID
Regulation Number
888.3040
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional
Size
Outer Diameter — 9 Millimeter
Length — 30 Millimeter
Length — 20 Millimeter
Length — 25 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIb
GUDID
Class II

Manufacturer details

EUDAMED SRN
US-MF-000012663
Authorised representative
MDSS GmbH DE-AR-000005430

Related devices

Category: Tendon/ligament bone anchor, non-bioabsorbable

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (18)

  • 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
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No