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Dte

FDA UDI

Class I (US FDA UDI)

by Guilin Woodpecker Medical Instrument Co., Ltd.

Identity

Trade Name
DTE FDA UDI
Generic Name
Dental irrigation/aspiration syringe FDA UDI
Device Name
Syringe, dental, irrigating FDA UDI
Model / Reference
Endo 1 FDA UDI
Description
Syringe, dental, irrigating FDA UDI

Identifiers

Primary DI / UDI-DI
06944843603223 FDA UDI
FDA Product Code
JET FDA UDI
GMDN Term
Dental irrigation/aspiration syringe FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6650 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental irrigation/aspiration syringe

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

Similar devices

Also classified as Dental irrigation/aspiration syringe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ce795801-2fec-4203-a614-410b6106e095 33 fields · synced May 30, 2026