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CryoProbe

FDA UDI

Class II (US FDA UDI)

by H & O Equipments SA

Identity

Trade Name
CryoProbe FDA UDI
Generic Name
Nitrous oxide gas cartridge FDA UDI
Model / Reference
N2O 8g cartridges and filters FDA UDI

Identifiers

Catalog Number
S-NOR10 FDA UDI
Primary DI / UDI-DI
B386SNOR101 FDA UDI
510(k) Number
K024009 FDA UDI
FDA Product Code
GEH FDA UDI
GMDN Term
Nitrous oxide gas cartridge FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4350 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nitrous oxide gas cartridge

CryoProbe by H & O Equipments SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nitrous oxide gas cartridge.

Cleared under the same submission

K024009 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
H & O Equipments SA

Sources (1)

  • FDA UDI 4528704d-3217-4d5b-a71a-0d8877db6320 35 fields · synced May 30, 2026