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Provisa

FDA UDI

Class I (US FDA UDI)

by Benco Dental Supply Co.

Identity

Trade Name
PROVISA FDA UDI
Generic Name
Dental material injection cannula, reusable FDA UDI
Device Name
PROVISA CEM SE MIX TIPS #15 50 FDA UDI
Model / Reference
4985-162 FDA UDI
Description
PROVISA CEM SE MIX TIPS #15 50 FDA UDI

Identifiers

Primary DI / UDI-DI
D74449851620 FDA UDI
FDA Product Code
EJB FDA UDI
GMDN Term
Dental material injection cannula, reusable 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

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

No

FDA UDI

Category: Dental material injection cannula, reusable

Provisa by Benco Dental Supply Co. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental material injection cannula, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2d277698-79ee-4b48-8f3e-a2d896697575 33 fields · synced May 30, 2026