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Roott

FDA UDI

Class I (US FDA UDI)

by Trate Llc

Identity

Trade Name
ROOTT FDA UDI
Generic Name
Manual non-rotary dental instrument handle FDA UDI
Device Name
Surgical handle, handpiece. FDA UDI
Model / Reference
ETH FDA UDI
Description
Surgical handle, handpiece. FDA UDI

Identifiers

Primary DI / UDI-DI
00810149980725 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Manual non-rotary dental instrument handle FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Manual non-rotary dental instrument handle

Roott by Trate Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual non-rotary dental instrument handle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Trate Llc

Sources (1)

  • FDA UDI 32d4026a-ed31-437b-8d28-6432807c2116 34 fields · synced Jun 8, 2026