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Woodpecker

FDA UDI

Class I (US FDA UDI)

by Guilin Woodpecker Medical Instrument Co., Ltd.

Identity

Trade Name
WOODPECKER FDA UDI
Generic Name
Gutta-percha injector FDA UDI
Device Name
Gutta-percha injector FDA UDI
Model / Reference
WP5004 FDA UDI
Description
Gutta-percha injector FDA UDI

Identifiers

Primary DI / UDI-DI
06944843604428 FDA UDI
FDA Product Code
EKR FDA UDI
GMDN Term
Gutta-percha injector FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Gutta-percha injector

Woodpecker by Guilin Woodpecker Medical Instrument Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gutta-percha injector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Guilin Woodpecker Medical Instrument Co., Ltd.

Sources (1)

  • FDA UDI 32ee2652-3664-4546-982a-fe373dd9c57d 33 fields · synced Jun 8, 2026