Hoc2 A.r.t. Of C.c.d. ®with Valve Soft Plug

FDA UDI

Class II (US FDA UDI)

by Laboratoire Ccd

Identity

Trade Name: HOC2 A.R.T. OF C.C.D. ®WITH VALVE SOFT PLUG FDA UDI
Generic Name: IVF oocyte aspiration needle, single-use FDA UDI
Device Name: Set for oocyte retrieval FDA UDI
Model / Reference: HOC2 A.R.T. OF C.C.D. ®WITH VALVE SOFT PLUG FDA UDI
Description: Set for oocyte retrieval FDA UDI

Identifiers

Catalog Number: 1313601 FDA UDI
Primary DI / UDI-DI: 03700111400962 FDA UDI
FDA Product Code: MQE FDA UDI
GMDN Term: IVF oocyte aspiration needle, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 884.6100 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: Shaft Length — 30 Centimeter FDA UDI
Needle Gauge — 17 Gauge FDA UDI

Category: IVF oocyte aspiration needle, single-use

Hoc2 A.r.t. Of C.c.d. ®with Valve Soft Plug 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 d1b900d8-2b2e-4c41-a936-c5ac2efb5fcd 37 fields · synced May 30, 2026