FDA UDI In Commercial Distribution 🇺🇸 United States

BioFire® Respiratory Panel 2.1

DI: 00815381020529 · Model: 423742 · BIOFIRE DIAGNOSTICS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BioFire® Respiratory Panel 2.1
Primary DI
00815381020529
Version / Model
423742
Company Name
BIOFIRE DIAGNOSTICS, LLC
Labeler DUNS
079280262
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-04-13
Public Version
1
Public Version Date
2021-04-21
Public Version Status
New
Public Device Record Key
e2b3cbad-bacc-4502-a2c5-1240b0b756f8

Device Description

IVD reagent kit containing 30 tests.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
No
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
QOF Multi-Target Respiratory Specimen Nucleic Acid Test Including Sars-Cov-2 And Other Microbial Agents

GMDN Terms

Code Name
61527 Multiple-type respiratory pathogen nucleic acid IVD, kit, nucleic acid technique (NAT)

Identifiers

Type ID
Primary 00815381020529

Premarket Submissions

Submission Number Supplement Number
DEN200031 000