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Parkell®

FDA UDI

Class II (US FDA UDI)

by Parkell, Inc.

Identity

Trade Name
Parkell® FDA UDI
Generic Name
Dental etching solution FDA UDI
Device Name
Parkell® Etching Gel FDA UDI
Model / Reference
S276 FDA UDI
Description
Parkell® Etching Gel FDA UDI

Identifiers

Catalog Number
S276 FDA UDI
Primary DI / UDI-DI
10810000527554 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Dental etching solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3275 FDA UDI
Commercial Distribution
Not 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

Parkell® by Parkell, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Parkell, Inc.

Sources (1)

  • FDA UDI 91c96e37-29a0-48b7-b4dc-9d0476c1eff0 37 fields · synced May 31, 2026