← Back to catalogue

Anthogyr OSTEO SAFE

FDA UDI

Class I (US FDA UDI)

by Etablissements Anthogyr

Identity

Trade Name
Anthogyr OSTEO SAFE FDA UDI
Generic Name
Dental ultrasonic surgical system FDA UDI
Model / Reference
6920OSTS FDA UDI

Identifiers

Catalog Number
6920OSTS FDA UDI
Primary DI / UDI-DI
03663394482349 FDA UDI
FDA Product Code
EMM FDA UDI
GMDN Term
Dental ultrasonic surgical system 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental ultrasonic surgical system

Anthogyr OSTEO SAFE by Etablissements Anthogyr — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental ultrasonic surgical system.

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 2b949bcc-cf93-48ff-bcf6-e31160018d7e 34 fields · synced May 29, 2026