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RFB-03-0200-00 (Rectifier-Board)

FDA UDI

Class I (US FDA UDI)

by W & H Dentalwerk Bürmoos GmbH

Identity

Trade Name
RFB-03-0200-00 (Rectifier-Board) FDA UDI
Generic Name
Dental delivery system instrument unit, electric FDA UDI
Device Name
Built-in Component FDA UDI
Model / Reference
30348000 FDA UDI
Description
Built-in Component FDA UDI

Identifiers

Primary DI / UDI-DI
J021303480001 FDA UDI
FDA Product Code
EIA FDA UDI
ELC FDA UDI
GMDN Term
Dental delivery system instrument unit, electric FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 FDA UDI
872.4850 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, electric

RFB-03-0200-00 (Rectifier-Board) 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, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
W & H Dentalwerk Bürmoos GmbH

Sources (1)

  • FDA UDI d3382f7a-faf3-4ca8-9f1b-1853acc6d330 33 fields · synced Jun 1, 2026