Hoc Collection Vial 30ml

FDA UDI

Class II (US FDA UDI)

by Laboratoire Ccd

Identity

Trade Name: HOC COLLECTION VIAL 30ML FDA UDI
Generic Name: Assisted reproduction cryotube FDA UDI
Device Name: Device for oocyte collection FDA UDI
Model / Reference: HOC COLLECTION VIAL 30ML FDA UDI
Description: Device for oocyte collection FDA UDI

Identifiers

Catalog Number: 1302001 FDA UDI
Primary DI / UDI-DI: 03700111400863 FDA UDI
FDA Product Code: MQE FDA UDI
GMDN Term: Assisted reproduction cryotube 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

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: Total Volume — 30 Milliliter FDA UDI

Category: Assisted reproduction cryotube

Hoc Collection Vial 30ml by Laboratoire Ccd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assisted reproduction cryotube.

LabChoice Cryogenic Tubes, With Graduated Markings, 5mL, Sterile — Dynarex Corp. · Class I
LabChoice Cryogenic Tubes, With Graduated Markings, 2mL, Sterile — Dynarex Corp. · Class I
CryoTip® — FUJIFILM IRVINE SCIENTIFIC, INC. · Class II

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Laboratoire Ccd

Sources (1)

FDA UDI ebbf86b1-9336-4160-b786-593ba7681552 37 fields · synced Jun 1, 2026