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Drill Bit

by Shenzhen World Surgery Medical Device Technology Co., Ltd. 84 variants

Ref WDTO00221, WDTO00390, WDTO00405, WDTO00178, WDTO00349, WDTO00385, WDTO00027, WDTO00145, WDTO00407, WDTO00179, WDTO00384, WDTO00164, WDTO00180, WDTO09029, WDTO00455, WDTO00032, WDTO00017, WDTO09147, WDTO00077, WDTO00014, WDTO00447, WDTO00335, WDTO00217, WDTO02100, WDTO00183, WDTO09143, WDTO00381, WDTO00055, WDTO00115, WDTO00169, WDTO00387, WDTO09139, WDTO00339, WDTO00177, WDTO09030, WDTO00011, WDTO09146, WDTO00176, WDTO00161, WDTO09028, WDTO00026, WDTO00336, WDTO00131, WDTO00132, WDTO00403, WDTO00025, WDTO00144, WDTO00418, WDTO00029, WDTO00015, WDTO00219

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number695029260003012K2 Basic UDI-DI Date7 Apr 2026RegisteredStatusActive

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

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Drill Bit
Model / Reference
WDTO00221, WDTO00390, WDTO00405, WDTO00178, WDTO00349, WDTO00385, WDTO00027, WDTO00145, WDTO00407, WDTO00179, WDTO00384, WDTO00164, WDTO00180, WDTO09029, WDTO00455, WDTO00032, WDTO00017, WDTO09147, WDTO00077, WDTO00014, WDTO00447, WDTO00335, WDTO00217, WDTO02100, WDTO00183, WDTO09143, WDTO00381, WDTO00055, WDTO00115, WDTO00169, WDTO00387, WDTO09139, WDTO00339, WDTO00177, WDTO09030, WDTO00011, WDTO09146, WDTO00176, WDTO00161, WDTO09028, WDTO00026, WDTO00336, WDTO00131, WDTO00132, WDTO00403, WDTO00025, WDTO00144, WDTO00418, WDTO00029, WDTO00015, WDTO00219
Primary DI / UDI-DI
06950292699809, 06950292664579, 06950292663381, 06950292683693, 06950292699908, 06950292664524, 06950292663664, 06950292683563, 06950292663428, 06950292683709, 06950292664517, 06950292683617, 06950292683716, 06950292674738, 06950292680265, 06950292680258, 06950292663411, 06950292667686, 06950292663824, 06950292663350, 06950292664845, 06950292664326, 06950292664128, 06950292664883, 06950292680289, 06950292667648, 06950292664494, 06950292663732, 06950292699755, 06950292683662, 06950292664548, 06950292667617, 06950292664364, 06950292683686, 06950292674745, 06950292665729, 06950292667679, 06950292683679, 06950292664036, 06950292674721, 06950292663657, 06950292664333, 06950292681323, 06950292631991, 06950292663343, 06950292663640, 06950292683501, 06950292664678, 06950292663688, 06950292663374, 06950292699786
Basic UDI-DI
695029260003012K2
Direct Marketing DI
06950292699809
06950292664579
06950292663381
06950292683693
06950292699908
06950292664524
06950292663664
06950292683563
06950292663428
06950292683709
06950292664517
06950292683617
06950292683716
06950292674738
06950292680265
06950292680258
06950292663411
06950292667686
06950292663824
06950292663350
06950292664845
06950292664326
06950292664128
06950292664883
06950292680289
06950292667648
06950292664494
06950292663732
06950292699755
06950292683662
06950292664548
06950292667617
06950292664364
06950292683686
06950292674745
06950292665729
06950292667679
06950292683679
06950292664036
06950292674721
06950292663657
06950292664333
06950292681323
06950292631991
06950292663343
06950292663640
06950292683501
06950292664678
06950292663688
06950292663374
06950292699786
EMDN Code
L0916 Orthopaedic surgery burs and tips, reusable
Device Class
Class I
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
CN-MF-000017319
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Shenzhen World Surgery Medical Device Technology Co., Ltd.

See all devices from Shenzhen World Surgery Medical Device Technology Co., Ltd. →

Properties

  • Reusable

Other properties (12)

  • Sterile: 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