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Osteo-Force

FDA UDI

Class I (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Osteo-Force FDA UDI
Generic Name
Closed-wound drain connection tubing set FDA UDI
Device Name
Osteo-Force Connecting Tube FDA UDI
Model / Reference
G13344 FDA UDI
Description
Osteo-Force Connecting Tube FDA UDI

Identifiers

Catalog Number
TCT12.4-15-P-FMRA-HPIS FDA UDI
Primary DI / UDI-DI
00827002133440 FDA UDI
FDA Product Code
OAR FDA UDI
GMDN Term
Closed-wound drain connection tubing set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4200 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: Closed-wound drain connection tubing set

Osteo-Force by Cook Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Closed-wound drain connection tubing set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI 30dce2b0-eb0e-4bc3-a180-de01c693127a 36 fields · synced Jun 8, 2026