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Analog for Multi Unit

FDA UDI

Class I (US FDA UDI)

by Rdj Tov Implant, Ltd.

Identity

Trade Name
Analog for Multi Unit FDA UDI
Generic Name
Dental implant system FDA UDI
Model / Reference
10mm FDA UDI

Identifiers

Catalog Number
AMU FDA UDI
Primary DI / UDI-DI
07290117800911 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant system 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

Yes

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant system

Analog for Multi Unit by Rdj Tov Implant, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d3983dd6-f590-4c52-a359-2c792cd3c066 33 fields · synced May 30, 2026