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Microprime

FDA UDI

Class II (US FDA UDI)

by Danville Materials, Llc

Identity

Trade Name
MICROPRIME FDA UDI
Generic Name
Dental coating, tooth-desensitizing FDA UDI
Device Name
MICROPRIME B,10ML,FA FDA UDI
Model / Reference
87001 FDA UDI
Description
MICROPRIME B,10ML,FA FDA UDI

Identifiers

Catalog Number
87001 FDA UDI
Primary DI / UDI-DI
00816594021600 FDA UDI
FDA Product Code
KLE FDA UDI
GMDN Term
Dental coating, tooth-desensitizing 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

Yes

FDA UDI

Category: Dental coating, tooth-desensitizing

Microprime by Danville Materials, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental coating, tooth-desensitizing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a9f6f7f7-778d-4d0c-9ee9-c333f3780aaa 36 fields · synced May 30, 2026