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Memory Intra Uterine Insimination Cannula

FDA UDI

Class II (US FDA UDI)

by Laboratoire Ccd

Identity

Trade Name
MEMORY INTRA UTERINE INSIMINATION CANNULA FDA UDI
Generic Name
Assisted reproduction transfer catheter/set FDA UDI
Device Name
Catheter /probe for artificial insemination FDA UDI
Model / Reference
MEMORY INTRA UTERINE INSEMINATION CANNULA FDA UDI
Description
Catheter /probe for artificial insemination FDA UDI

Identifiers

Catalog Number
12040MF FDA UDI
Primary DI / UDI-DI
03700111400573 FDA UDI
FDA Product Code
HDR FDA UDI
GMDN Term
Assisted reproduction transfer catheter/set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5250 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

No

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

Yes

FDA UDI

Dimensions & Sizes

Size
Catheter Length — 18 Centimeter FDA UDI
Outer Diameter — 0.21 Centimeter FDA UDI

Category: Assisted reproduction transfer catheter/set

Memory Intra Uterine Insimination Cannula by Laboratoire Ccd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assisted reproduction transfer catheter/set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Laboratoire Ccd

Sources (1)

  • FDA UDI c8577622-f362-4c66-ad68-1cab1364e514 37 fields · synced May 29, 2026