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Two Striper

FDA UDI

Class I (US FDA UDI)

by Abrasive Technology, Llc

Identity

Trade Name
Two Striper FDA UDI
Generic Name
Polymeric dental bur FDA UDI
Device Name
Abrasive Point FDA UDI
Model / Reference
STAINBUSTER 2505 6-BUR PACK FDA UDI
Description
Abrasive Point FDA UDI

Identifiers

Catalog Number
C840043 FDA UDI
Primary DI / UDI-DI
B868C8400431 FDA UDI
FDA Product Code
EHL FDA UDI
GMDN Term
Polymeric dental bur FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6010 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Polymeric dental bur

Two Striper by Abrasive Technology, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polymeric dental bur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7ab1016b-1757-4e61-a868-9179651aa202 34 fields · synced May 31, 2026