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Minikut

FDA UDI

Class I (US FDA UDI)

by Sure Dent Corporation

Identity

Trade Name
Minikut FDA UDI
Generic Name
Synthetic gutta-percha FDA UDI
Device Name
Bio Gutta Percha Points Taper .05, Size 40, 60/PK, mm marked, SB FDA UDI
Model / Reference
G906 LB40.05 FDA UDI
Description
Bio Gutta Percha Points Taper .05, Size 40, 60/PK, mm marked, SB FDA UDI

Identifiers

Catalog Number
1600540CT FDA UDI
Primary DI / UDI-DI
08800069202672 FDA UDI
FDA Product Code
EKM FDA UDI
GMDN Term
Synthetic gutta-percha FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Synthetic gutta-percha

Minikut by Sure Dent Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synthetic gutta-percha.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI abc329d5-25ee-4c38-8c42-c4a4c5c20214 35 fields · synced Jun 6, 2026