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Revo

by Conmed Corporation 2 variants

Ref C6102B, C6101A, C6101H, C6107

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 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 Number084585408435DB Basic UDI-DI Date30 Apr 2026RegisteredStatusActive
European UnionCE/MDR EUDAMED Number084585408435DB Basic UDI-DI Date30 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854026717 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  • Withdrawn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, CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Revo
Revo, Hi-Fi
Generic Name
Tendon/ligament bone anchor, non-bioabsorbable
Bone-coring punch, reusable
Orthopaedic implant driver
Device Name
Orthopedic, Non-active, Reusable Surgical Instrument, Passing/Retrieval
Orthopedic, Implant, Non-absorbable, Suture Anchor, Titanium, Shoulder, REVO/Mini-REVO
Reusable Manual Surgical Instruments
Model / Ref / Catalog
C6102B, C6101A, C6101H, C6107
Primary DI / UDI-DI
10845854026717, 10845854015070, 20845854019785, 10845854030707
Basic UDI-DI
084585408435DB, B-10845854015070, B-20845854019785, B-10845854030707
Direct Marketing DI
20845854026714
510(k) Number
FDA Product Code
MBI, MDM, GFG
EMDN Code
L091001, P09120102, L0999
GMDN Term
Tendon/ligament bone anchor, non-bioabsorbable
Bone-coring punch, reusable
Orthopaedic implant driver
Device Class
Class I EUDAMEDGUDID
Class IIb EUDAMED
Class II GUDID
Regulation Number
888.3040, 878.4800, 878.4820
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
MRI Safety
MR Conditional
Size
Outer Diameter — 4 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class I
Class IIb
GUDID
Class I
Class II

Manufacturer details

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

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Sterile NoEUDAMEDGUDIDYesEUDAMEDGUDID
  • Single Use YesGUDIDNoGUDID
  • Implantable NoEUDAMEDGUDIDYesEUDAMEDGUDID
  • Reusable NoEUDAMEDYesEUDAMED
  • Prescription Use
  • Premarket Exempt NoGUDIDYesGUDID
  • Lot / Batch Number
  • Expiration Date YesGUDIDNoGUDID
  • Manufacturing Date NoGUDIDYesGUDID

Other properties (15)

  • 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
  • Serial Number: No