← Back to catalogue

Air-Flow

FDA UDI

Class I (US FDA UDI)

by E.M.S. Electro Medical Systems S.A.

Identity

Trade Name
AIR-FLOW FDA UDI
Generic Name
Professional dental abrasive material FDA UDI
Device Name
4 bottles 300g powder AIR-FLOW CLASSIC Cherry FDA UDI
Model / Reference
DV-164/A/CHE FDA UDI
Description
4 bottles 300g powder AIR-FLOW CLASSIC Cherry FDA UDI

Identifiers

Primary DI / UDI-DI
07613353197148 FDA UDI
FDA Product Code
EJR FDA UDI
GMDN Term
Professional dental abrasive material FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6030 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Professional dental abrasive material

Air-Flow by E.M.S. Electro Medical Systems S.A. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Professional dental abrasive material.

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 d0fef81d-5a4e-49cb-a267-8db40476aa89 34 fields · synced Jun 8, 2026