← Back to catalogue

Dental Electric Motor

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref MT3

by Guilin Woodpecker Medical Instrument Co., Ltd.

Identity

Trade Name
Dental Electric Motor EUDAMED
DTE,WOODPECKER FDA UDI
Generic Name
Dental delivery system instrument unit, electric FDA UDI
Device Name
Dental Electric Motor EUDAMED
Dental delivery system instrument unit, electric FDA UDI
Model / Reference
MT3 EUDAMEDFDA UDI
Description
Dental delivery system instrument unit, electric FDA UDI

Identifiers

Primary DI / UDI-DI
06944843611259 EUDAMEDFDA UDI
Basic UDI-DI
694484360517KY EUDAMED
510(k) Number
K203706 FDA UDI
FDA Product Code
EGS FDA UDI
EBW FDA UDI
EMDN Code
Z12110101 DENTAL TREATMENT UNITS EUDAMED
GMDN Term
Dental delivery system instrument unit, electric FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
872.4200 FDA UDI
Market of Registration
Northern Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental delivery system

Dental Electric Motor by Guilin Woodpecker Medical Instrument Co., Ltd. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental delivery system.

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

EUDAMED SRN
CN-MF-000009139
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (2)

  • EUDAMED 80263c2d-563d-4dfa-8db7-43b2c6696b49 61 fields · synced Oct 6, 2026
  • FDA UDI 5c9ddcb1-28fc-4f8c-87c1-b98b8de44db6 34 fields · synced May 30, 2026