FDA UDI In Commercial Distribution 🇺🇸 United States

Exact Diagnostics

DI: 00812242031007 · Model: HPVP200 · EXACT DIAGNOSTICS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Exact Diagnostics
Primary DI
00812242031007
Version / Model
HPVP200
Catalog Number
HPVP200
Company Name
EXACT DIAGNOSTICS, LLC
Labeler DUNS
079898166
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-06-17
Public Version
1
Public Version Date
2022-06-27
Public Version Status
New
Public Device Record Key
5d0d2e7e-98be-47ee-80fe-f6672543b711

Device Description

HPV Verification Panel

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 00812242031007

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius