← Back to catalogue

Lares Research

FDA UDI

Class I (US FDA UDI)

by Lares Research, Inc.

Identity

Trade Name
Lares Research FDA UDI
Generic Name
Surgical power tool system control unit, line-powered FDA UDI
Device Name
Electric Motor and Control, ProStyle E, 1000-40000 rpm FDA UDI
Model / Reference
Motor/Control, ProStyle E, Electric FDA UDI
Description
Electric Motor and Control, ProStyle E, 1000-40000 rpm FDA UDI

Identifiers

Catalog Number
13177 FDA UDI
Primary DI / UDI-DI
D9501317701 FDA UDI
FDA Product Code
EIA FDA UDI
GMDN Term
Surgical power tool system control unit, line-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Lares Research by Lares Research, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 9d4f408d-2298-461e-bdf4-b93812df196b 36 fields · synced May 31, 2026