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Power Dental USA

FDA UDI

Class I (US FDA UDI)

by Power Dental USA, Inc.

Identity

Trade Name
Power Dental USA FDA UDI
Generic Name
Dental anaesthesia syringe, reusable FDA UDI
Device Name
SYRINGES ASPIRATED 2.2ml WING, RECOMMEND USE OF PLASTIC NEEDLES (NOT ALUMINIUM) FDA UDI
Model / Reference
7018L FDA UDI
Description
SYRINGES ASPIRATED 2.2ml WING, RECOMMEND USE OF PLASTIC NEEDLES (NOT ALUMINIUM) FDA UDI

Identifiers

Catalog Number
7018L FDA UDI
Primary DI / UDI-DI
D9437018L00 FDA UDI
FDA Product Code
EIC FDA UDI
GMDN Term
Dental anaesthesia syringe, reusable 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

No

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental anaesthesia syringe, reusableDental irrigation/aspiration syringe

Power Dental USA by Power Dental USA, Inc. — 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 dc46739e-2283-42fe-847a-6e958f30d7c4 35 fields · synced Jun 1, 2026