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Sequent

by Conmed Corporation 2 variants

Ref SCEC047, MR004C, MR003C

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-10845854040416 Basic UDI-DI Date6 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854040416 UDI-DI Date13 Oct 2021ListedStatusListed 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  • Withdrawn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
Arthroscopic surgical procedure kit, non-medicated, single-use
Suturing unit, single-use
Device Name
Orthopedic, Non-active, Surgical Procedure Kit, Sequent
Orthopedic, Implant, Non-absorbable, Suture Anchor, PEEK, Knee, Sequent
Model / Ref / Catalog
SCEC047, MR004C, MR003C
Primary DI / UDI-DI
10845854040416, 20845854036584, 20845854036577
Basic UDI-DI
B-10845854040416, B-20845854036584, B-20845854036577
510(k) Number
FDA Product Code
KDQ, MBI, GAT
EMDN Code
T0202, P09120102
GMDN Term
Arthroscopic surgical procedure kit, non-medicated, single-use
Suturing unit, single-use
Device Class
Class IIa EUDAMED
Class IIb EUDAMED
Class II GUDID
Regulation Number
880.6740, 888.3040, 878.5000
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
Class IIb
GUDID
Class II
ImplantableEUDAMED
No
Yes
GUDID
No

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
  • Single Use
  • Implantable NoEUDAMEDGUDIDYesEUDAMED
  • Prescription Use
  • Premarket Exempt YesGUDIDNoGUDID
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date NoGUDIDYesGUDID

Other properties (16)

  • 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
  • Serial Number: No