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HE-43 T SD Alegra Handpiece

FDA UDI

Class I (US FDA UDI)

by W & H Dentalwerk Bürmoos GmbH

Identity

Trade Name
HE-43 T SD Alegra Handpiece FDA UDI
Generic Name
Dental surgical power tool motorized handpiece/set, electric FDA UDI
Device Name
Alegra Handpiece Attachment FDA UDI
Model / Reference
30129000 FDA UDI
Description
Alegra Handpiece Attachment FDA UDI

Identifiers

Primary DI / UDI-DI
J021301290001 FDA UDI
FDA Product Code
EFB FDA UDI
GMDN Term
Dental surgical power tool motorized handpiece/set, electric FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 FDA UDI
Commercial Distribution
Not 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

HE-43 T SD Alegra Handpiece by W & H Dentalwerk Bürmoos GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f6261b57-2070-49bf-b127-adb97164d2c3 34 fields · synced Jun 1, 2026