FDA UDI In Commercial Distribution 🇺🇸 United States

QC Sets and Panels: Helix Elite™

DI: 70845357043084 · Model: 8235 · MICROBIOLOGICS INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
QC Sets and Panels: Helix Elite™
Primary DI
70845357043084
Version / Model
8235
Catalog Number
8235
Company Name
MICROBIOLOGICS INC.
Labeler DUNS
060467826
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-30
Public Version
1
Public Version Date
2020-05-08
Public Version Status
New
Public Device Record Key
c98932ed-5e3d-4ac8-a605-14e8fcbf50c4

Device Description

QC Sets and Panels: Helix Elite™ Multi-Strain Human Papillomavirus (HPV) Verification Panel (Inactivated Pellet)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
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
52768 Human papillomavirus (HPV) nucleic acid IVD, control

Identifiers

Type ID
Primary 70845357043084

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 25 Degrees Celsius