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Sweden & Martina

by Sweden & Martina S.P.A.

Ref U-CAMC-430-10-SW, YV-DR-N-CA-L, E-MPSCR-410, AS-MPSCI-425, PAD-VM-180, LS-TCIN-380-10-8, AS-CAMT-425-8-SW, M2300531Model Prosthetic Component, Surgical Instrument, Root Canal Instruments

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 22 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-+D7701581903 Basic UDI-DI Date11 Jul 2024RegisteredStatusActive
United StatesGUDID listing GUDID Number+D7701581903 UDI-DI Date14 Feb 2018ListedStatusListed 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 22 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  • Withdrawn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

Trade Name
Sweden & Martina EUDAMED
Pre-Made Rep. Post Anatomical GUDID
Generic Name
Dental implant suprastructure, permanent, preformed
Model / Ref / Catalog
Prosthetic Component EUDAMED
U-CAMC-430-10-SW EUDAMED
Surgical Instrument EUDAMED
YV-DR-N-CA-L EUDAMED
E-MPSCR-410 EUDAMED
AS-MPSCI-425 EUDAMED
PAD-VM-180 EUDAMED
LS-TCIN-380-10-8 EUDAMED
AS-CAMT-425-8-SW EUDAMED
Root Canal Instruments EUDAMED
M2300531 EUDAMED
AS-MDR-425-1 GUDID
Primary DI / UDI-DI
+D7701581903 EUDAMED
+D7702482653 EUDAMED
+D7700879493 EUDAMED
+D7701245643 EUDAMED
+D7700830423 EUDAMED
+D7702309883 EUDAMED
+D7701592653 EUDAMED
+D7700670453 EUDAMED
D7701245683 GUDID
Basic UDI-DI
B-+D7701581903, B-+D7702482653, B-+D7700879493, B-+D7701245643, B-+D7700830423, B-+D7702309883, B-+D7701592653, B-+D7700670453
510(k) Number
FDA Product Code
NHA
EMDN Code
P010299, L159099, Q010199
GMDN Term
Dental implant suprastructure, permanent, preformed
Device Class
Class IIa EUDAMED
Class IIb EUDAMED
Class II GUDID
Regulation Number
872.3630
EU market of registration
Italy
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 5 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
Prosthetic Component
U-CAMC-430-10-SW
Surgical Instrument
YV-DR-N-CA-L
E-MPSCR-410
AS-MPSCI-425
PAD-VM-180
LS-TCIN-380-10-8
AS-CAMT-425-8-SW
Root Canal Instruments
M2300531
GUDID
AS-MDR-425-1
Primary DI / UDI-DIEUDAMED
+D7701581903
+D7702482653
+D7700879493
+D7701245643
+D7700830423
+D7702309883
+D7701592653
+D7700670453
GUDID
D7701245683
Device ClassEUDAMED
Class IIa
Class IIb
GUDID
Class II
SterileEUDAMED
Yes
No
GUDID
No
ImplantableEUDAMED
No
GUDID
Yes

Manufacturer details

EUDAMED SRN
IT-MF-000007391

Other devices from Sweden & Martina S.P.A.

See all devices from Sweden & Martina S.P.A. →

Properties

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

Other properties (15)

  • 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
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Manufacturing Date: No