FDA UDI Not in Commercial Distribution 🇺🇸 United States

QC Sets and Panels: Helix Elite™

DI: 70845357043053 · Model: 8240 · MICROBIOLOGICS INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
QC Sets and Panels: Helix Elite™
Primary DI
70845357043053
Version / Model
8240
Catalog Number
8240
Company Name
MICROBIOLOGICS INC.
Labeler DUNS
060467826
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-30
Public Version
3
Public Version Date
2024-11-27
Public Version Status
Update
Public Device Record Key
01e77fc5-b6cc-495b-a76a-a76c6f1f91b3
Distribution End Date
2022-05-16

Device Description

QC Sets and Panels: Helix Elite™ Mycoplasma genitalium Control Panel (Inactivated Pellet)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OHQ Multi-analyte controls unassayed

GMDN Terms

Code Name
47323 Mycoplasma genitalium nucleic acid IVD, control

Identifiers

Type ID
Primary 70845357043053

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 25 Degrees Celsius