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Duro-Ject

FDA UDI

Class I (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Duro-Ject FDA UDI
Generic Name
Non-ISO80369-standardized small-bore linear connector, single-use FDA UDI
Device Name
Duro-Ject Curved Connecting Tube FDA UDI
Model / Reference
G36272 FDA UDI
Description
Duro-Ject Curved Connecting Tube FDA UDI

Identifiers

Catalog Number
TCT9.9-29-P-FMRA-DURO FDA UDI
Primary DI / UDI-DI
00827002362727 FDA UDI
FDA Product Code
OAR FDA UDI
GMDN Term
Non-ISO80369-standardized small-bore linear connector, single-use 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: Non-ISO80369-standardized small-bore linear connector, single-use

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

Similar devices

Also classified as Non-ISO80369-standardized small-bore linear connector, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI 826c89d8-9112-46ef-85a5-7bf0ec5254de 36 fields · synced Jun 8, 2026