← Back to catalogue

AC-1.0 Advanced Air

FDA UDI

Class I (US FDA UDI)

by W & H Dentalwerk Bürmoos GmbH

Identity

Trade Name
AC-1.0 Advanced Air FDA UDI
Generic Name
Dental delivery system instrument unit, pneumatic FDA UDI
Device Name
Electronic for Advanced Air FDA UDI
Model / Reference
30223000 FDA UDI
Description
Electronic for Advanced Air FDA UDI

Identifiers

Primary DI / UDI-DI
J021302230001 FDA UDI
FDA Product Code
EFB FDA UDI
GMDN Term
Dental delivery system instrument unit, pneumatic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental delivery system instrument unit, pneumatic

AC-1.0 Advanced Air by W & H Dentalwerk Bürmoos GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental delivery system instrument unit, pneumatic.

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

Manufacturer
W & H Dentalwerk Bürmoos GmbH

Sources (1)

  • FDA UDI dcee6035-bca9-4d70-836d-bde096c7477e 33 fields · synced May 31, 2026