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Olcott

FDA UDI

Class I (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Olcott FDA UDI
Generic Name
Torque manipulation device FDA UDI
Device Name
Olcott Torque Device FDA UDI
Model / Reference
G13811 FDA UDI
Description
Olcott Torque Device FDA UDI

Identifiers

Catalog Number
OTD-100 FDA UDI
Primary DI / UDI-DI
00827002138117 FDA UDI
FDA Product Code
KGZ FDA UDI
GMDN Term
Torque manipulation device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Category: Torque manipulation device

Olcott by Cook Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Torque manipulation device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI bf25cbda-dfd1-42b3-80bf-bde85bcb485b 36 fields · synced Jun 8, 2026