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Benda Twin

FDA UDI

Class I (US FDA UDI)

by Centrix, Inc.

Identity

Trade Name
Benda Twin FDA UDI
Generic Name
Dental material application tool, single-use FDA UDI
Device Name
Benda Twin Pink FDA UDI
Model / Reference
370105 FDA UDI
Description
Benda Twin Pink FDA UDI

Identifiers

Primary DI / UDI-DI
00817051023427 FDA UDI
FDA Product Code
KXR FDA UDI
GMDN Term
Dental material application tool, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3140 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental material application tool, single-use

Benda Twin by Centrix, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental material application tool, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Centrix, Inc.

Sources (1)

  • FDA UDI b46fb8d3-4e9d-44b5-9dc3-9daf148d8e92 33 fields · synced Jun 1, 2026