← Back to catalogue

LHP-6 handpiece

FDA UDI

Class I (US FDA UDI)

by Osada Electric Co., Ltd.

Identity

Trade Name
LHP-6 handpiece FDA UDI
Generic Name
Dental laboratory drilling system handpiece FDA UDI
Model / Reference
LHP-6 FDA UDI

Identifiers

Catalog Number
82125 FDA UDI
Primary DI / UDI-DI
04582227341358 FDA UDI
FDA Product Code
EKX FDA UDI
GMDN Term
Dental laboratory drilling system handpiece FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 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

Yes

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
Liquid Chemical FDA UDI

Category: Dental laboratory drilling system handpiece

LHP-6 handpiece by Osada Electric Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental laboratory drilling system handpiece.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 2dd94c1b-8741-48a9-9019-7e8a7f21b349 33 fields · synced May 30, 2026