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Dolwick TMJ-Spreader Forceps 16cm/6¼", left

by IAA Surgical Instruments Company

Ref 21-200-01

Active European Union

CE MDR

Valid until

14 Jun 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier Intertek Medical Notified Body AB

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++B832RESURGICRETRACTORKL Basic UDI-DI +B83221200010SUDI-DIDate19 Jun 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Surgical Retractors
Model / Reference
21-200-01
Primary DI / UDI-DI
+B83221200010S
Basic UDI-DI
++B832RESURGICRETRACTORKL
Direct Marketing DI
+B83221200010S
EMDN Code
L150299 Odontostomatology spreaders and retractors, reusable - other
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
PK-MF-000023042
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Iaa Surgical Instruments Co

See all devices from Iaa Surgical Instruments Co →

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