FDA.report

HettCube

Primary DI
04050674070942
Brand
HettCube
Company
Andreas Hettich GmbH & Co. KG
Model
HettCube 600, 220-240V, 50/60 Hz
Catalog number
66000
Device description
A mains electricity (AC-powered) device intended to provide ideal conditions for the growth of microorganisms or mammalian cells in culture by automatically monitoring and controlling temperature, humidity, and gaseous conditions [e.g., carbon dioxide (CO2) and oxygen (O2) concentrations]. It typically consists of multiple shelves which hold cells in culture media (e.g., in microplates, petri dishes, flasks) and may have an integrated robotic transfer arm for loading and unloading the incubator onto other instruments in a clinical or research laboratory environment.
Published
2021-09-02
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
true
Sterile
false
Single use
false

Related Records

Product Codes

CodeName
JTQBath, Incubators/Water, All

Product Code Classifications

CodeDeviceSpecialtyClass
JTQBath, Incubators/Water, AllMicrobiology1

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
04050674070942PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedEAN-13
04050674070942040506740709424050674070942

GMDN Terms

TermDefinition
Automated laboratory incubatorA mains electricity (AC-powered) device intended to provide ideal conditions for the growth of microorganisms or mammalian cells in culture by automatically monitoring and controlling temperature, humidity, and gaseous conditions [e.g., carbon dioxide (CO2) and oxygen (O2) concentrations]. It typically consists of multiple shelves which hold cells in culture media (e.g., in microplates, petri dishes, flasks) and may have an integrated robotic transfer arm for loading and unloading the incubator onto other instruments in a clinical or research laboratory environment.

Sterilization Methods

Method

Regulatory Flags

DUNS number
316403245
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
Serial number
true
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

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