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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
bottle 20g AIR-FLOW CLASSIC powder Lemon FDA UDI
Model / Reference
A FDA UDI
Description
bottle 20g AIR-FLOW CLASSIC powder Lemon FDA UDI

Identifiers

Catalog Number
DV-1002 FDA UDI
Primary DI / UDI-DI
07613353154080 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

No

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

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Manufacturer

Sources (1)

  • FDA UDI 8941c419-0630-4928-a9d5-fd9212a0c742 35 fields · synced May 30, 2026