← Back to catalogue

RP 2.25mm Hex Handpiece Adapter FLX - Medium

FDA UDI

Class I (US FDA UDI)

by Adin Dental Implant Systems Ltd

Identity

Trade Name
RP 2.25mm Hex Handpiece Adapter FLX - Medium FDA UDI
Generic Name
Dental torque wrench FDA UDI
Model / Reference
RP0076 FDA UDI

Identifiers

Primary DI / UDI-DI
07290105159533 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental torque wrench FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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

Yes

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: Dental torque wrench

RP 2.25mm Hex Handpiece Adapter FLX - Medium by Adin Dental Implant Systems Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental torque wrench.

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 db067de2-40fb-4463-8587-8d155e5d9fa1 32 fields · synced May 30, 2026