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Endodontic Hand Instruments

FDA UDI

Class I (US FDA UDI)

by Tulsa Dental Products Llc

Identity

Trade Name
Endodontic Hand Instruments FDA UDI
Generic Name
Manual endodontic file/rasp, reusable FDA UDI
Device Name
BRASSELER REAMERS 25/08 FDA UDI
Model / Reference
82125008 FDA UDI
Description
BRASSELER REAMERS 25/08 FDA UDI

Identifiers

Catalog Number
82125008 FDA UDI
Primary DI / UDI-DI
D716821250081 FDA UDI
FDA Product Code
EKP FDA UDI
GMDN Term
Manual endodontic file/rasp, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Category: Manual endodontic file/rasp, reusable

Endodontic Hand Instruments by Tulsa Dental Products Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual endodontic file/rasp, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8d283238-6ede-41df-ba42-1760ee5745b6 34 fields · synced Jun 8, 2026