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Atip LFB

by Shining 3D Tech Co., Ltd. 2 variants

Ref 0837Model CS-A48-A，CS-A48-B，CS-A48-C，CS-A48-D，CS-A48-E，CS-A48-F，CS-A48-G，CS-A48-H，CS-A48-I，CS-A48-J，CS-A48-K,CS-A48-L,CS-A43-A,CS-A35-A,CS-A35-B，CS-A48M2-A

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

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

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
United StatesGUDID listing GUDID Number06942799000837 UDI-DI Date30 Jul 2026ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number697016308AoralscanElf7V Basic UDI-DI 06942799000837UDI-DIDate1 Sep 2025RegisteredStatusActive

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.

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade Name
Atip LFB EUDAMED
Marathon® GUDID
Generic Name
Dental milling system, CAD/CAM, chairside
Device Name
Scanbody
Model / Reference
CS-A48-A，CS-A48-B，CS-A48-C，CS-A48-D，CS-A48-E，CS-A48-F，CS-A48-G，CS-A48-H，CS-A48-I，CS-A48-J，CS-A48-K EUDAMED
CS-A48-L EUDAMED
CS-A43-A EUDAMED
CS-A35-A EUDAMED
CS-A35-B，CS-A48M2-A EUDAMED
0837 EUDAMED
Atip LFB GUDID
Primary DI / UDI-DI
06942799000837
Basic UDI-DI
697016308AoralscanElf7V
Direct Marketing DI
06942799000837
FDA Product Code
NOF
EMDN Code
Q0199 Odontology devices - other
GMDN Term
Dental milling system, CAD/CAM, chairside
Device Class
Class I EUDAMED
Class II GUDID
Regulation Number
872.3661
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class I
GUDID
Class II

Manufacturer details

EUDAMED SRN
CN-MF-000008402
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Shining 3D Tech Co., Ltd.

See all devices from Shining 3D Tech Co., Ltd. →

Properties

  • Reusable
  • Premarket Exempt
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (19)

  • 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
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No