← Back to catalogue

S/Etch

FDA UDI

Class II (US FDA UDI)

by Sdi , Ltd.

Identity

Trade Name
S/ETCH FDA UDI
Generic Name
Dental etching solution FDA UDI
Model / Reference
S/ETCH 4X1.2ML SYR MINI KT FDA UDI

Identifiers

Catalog Number
8100039 FDA UDI
Primary DI / UDI-DI
DO3681000391 FDA UDI
510(k) Number
K941899 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

Yes

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

S/Etch by Sdi , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental etching solution.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Sdi , Ltd.

Sources (1)

  • FDA UDI 1be4eebc-6fcd-4278-8d11-c2ae79db01d8 36 fields · synced May 31, 2026