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DenFil Etchant-37

FDA UDI

Class II (US FDA UDI)

by Vericom Co., Ltd.

Identity

Trade Name
DenFil Etchant-37 FDA UDI
Generic Name
Dental etching solution FDA UDI
Device Name
Phosphoric etching gel ; DenFil Etchant-37 3ml x 1 syringe FDA UDI
Model / Reference
ET103-R000 FDA UDI
Description
Phosphoric etching gel ; DenFil Etchant-37 3ml x 1 syringe FDA UDI

Identifiers

Primary DI / UDI-DI
08809254451697 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental etching solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 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

Yes

FDA UDI

Category: Dental etching solution

DenFil Etchant-37 by Vericom Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental etching solution.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vericom Co., Ltd.

Sources (1)

  • FDA UDI c9d75a92-4f87-4938-93d0-80fe190920c0 35 fields · synced Jun 8, 2026