← Back to catalogue

Instruments

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 03.333.210

by Tyber Medical

Identity

Trade Name
Cannulated Screw System + FDA UDI
Generic Name
Surgical countersink, single-use FDA UDI
Device Name
Instruments EUDAMED
CANN COUNTERSINK FOR 2.0MM HEADED CANN SCREW + / QC FDA UDI
Model / Reference
03.333.210 EUDAMEDFDA UDI
Description
CANN COUNTERSINK FOR 2.0MM HEADED CANN SCREW + / QC FDA UDI

Identifiers

Catalog Number
03.333.210 FDA UDI
Primary DI / UDI-DI
00819917026702 EUDAMEDFDA UDI
Basic UDI-DI
019644901457 EUDAMED
FDA Product Code
LXH FDA UDI
EMDN Code
Z12139099 VARIOUS ORTHOPAEDIC AND TRAUMATOLOGY INSTRUMENTS - OTHER EUDAMED
GMDN Term
Surgical countersink, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic guidewire, reusable

Instruments by Tyber Medical — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic guidewire, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Tyber Medical
EUDAMED SRN
US-MF-000011350
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (2)

  • EUDAMED b36dcffe-5166-4e55-a605-6be1680f2dbe 61 fields · synced Jun 8, 2026
  • FDA UDI d8e9d857-2388-4247-a892-e265a39663d1 35 fields · synced May 29, 2026