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E-On

FDA UDI

Class II (US FDA UDI)

by Benco Dental Supply Co.

Identity

Trade Name
E-ON FDA UDI
Generic Name
Dentine adhesive FDA UDI
Device Name
E-ON UNIVERSAL DC ACTIVATR FDA UDI
Model / Reference
4853-401 FDA UDI
Description
E-ON UNIVERSAL DC ACTIVATR FDA UDI

Identifiers

Primary DI / UDI-DI
D74448534010 FDA UDI
FDA Product Code
KLE FDA UDI
GMDN Term
Dentine adhesive FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3200 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dentine adhesive

E-On by Benco Dental Supply Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dentine adhesive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2077764f-1b39-4cc3-a1aa-33f4d0a3e566 34 fields · synced May 29, 2026