Full Echo®23 Cm

FDA UDI

Class II (US FDA UDI)

by Laboratoire Ccd

Identity

Trade Name: FULL ECHO®23 CM FDA UDI
Generic Name: Assisted reproduction transfer catheter trial FDA UDI
Device Name: 03 pieces sets for embryo transfer FDA UDI
Model / Reference: FULL ECHO®23 CM FDA UDI
Description: 03 pieces sets for embryo transfer FDA UDI

Identifiers

Catalog Number: 1326501 FDA UDI
Primary DI / UDI-DI: 03700111400412 FDA UDI
FDA Product Code: MQF FDA UDI
GMDN Term: Assisted reproduction transfer catheter trial FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 884.6110 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 0.155 Centimeter FDA UDI
Catheter Length — 29.5 Centimeter FDA UDI

Category: Assisted reproduction transfer catheter trial

Full Echo®23 Cm by Laboratoire Ccd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Laboratoire Ccd

Sources (1)

FDA UDI c805475b-568f-4263-b35d-00e0af48e8fa 37 fields · synced Jun 1, 2026