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Premier

FDA UDI

Class II (US FDA UDI)

by Premier Dental Products Company

Identity

Trade Name
Premier FDA UDI
Generic Name
Electrosurgical handpiece, single-use FDA UDI
Device Name
PENCIL- HANDSWITCHING, DISPOSABLE 5PK FDA UDI
Model / Reference
9006505 FDA UDI
Description
PENCIL- HANDSWITCHING, DISPOSABLE 5PK FDA UDI

Identifiers

Primary DI / UDI-DI
D6919006505 FDA UDI
510(k) Number
K945492 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical handpiece, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrosurgical handpiece, single-use

Premier by Premier Dental Products Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical handpiece, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1552e1a8-9e90-4492-8ab4-a1e14e905a81 34 fields · synced Jun 6, 2026