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ColpotomizOR Tube

FDA UDI

Class II (US FDA UDI)

by The O R Company Pty Ltd

Identity

Trade Name
ColpotomizOR Tube FDA UDI
Generic Name
Colpotomy tube FDA UDI
Device Name
45mm diameter trans-vaginal tube, 3 way valve, Silicone tie FDA UDI
Model / Reference
45mm FDA UDI
Description
45mm diameter trans-vaginal tube, 3 way valve, Silicone tie FDA UDI

Identifiers

Catalog Number
C45-TV FDA UDI
Primary DI / UDI-DI
09349967001455 FDA UDI
FDA Product Code
HEW FDA UDI
GMDN Term
Colpotomy tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1640 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 45 Millimeter FDA UDI

Category: Colpotomy tube

ColpotomizOR Tube by The O R Company Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Colpotomy tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6602f7fb-085b-4902-9d16-64b67664f5e7 35 fields · synced May 30, 2026