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BruxZir

FDA UDI

Class I (US FDA UDI)

by Prismatik Dentalcraft, Inc.

Identity

Trade Name
BruxZir FDA UDI
Generic Name
Dental material injection cannula, single-use FDA UDI
Device Name
25 Automix Applicator Tips FDA UDI
Model / Reference
70-25AM FDA UDI
Description
25 Automix Applicator Tips FDA UDI

Identifiers

Catalog Number
70-25AM FDA UDI
Primary DI / UDI-DI
D7457025AM1 FDA UDI
FDA Product Code
EID FDA UDI
GMDN Term
Dental material injection cannula, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

No

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 injection cannula, single-use

BruxZir by Prismatik Dentalcraft, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental material injection cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 06d19241-9102-4a1f-9e7f-a87e29abac14 35 fields · synced Jun 1, 2026