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Accurett

FDA UDI

Class II (US FDA UDI)

by H & O Equipments SA

Identity

Trade Name
Accurett FDA UDI
Generic Name
Carbon dioxide cartridge, non-sterile FDA UDI
Model / Reference
16g CO2 cartridges FDA UDI

Identifiers

Catalog Number
S-CO2-16G-BOX FDA UDI
Primary DI / UDI-DI
B386SCO216GBOX1 FDA UDI
510(k) Number
K161615 FDA UDI
FDA Product Code
GEH FDA UDI
GMDN Term
Carbon dioxide cartridge, non-sterile 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: Carbon dioxide cartridge, non-sterile

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

Cleared under the same submission

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 3b14a45b-92d5-46db-bd88-bef5c19b7a5b 35 fields · synced May 29, 2026