FDA UDI In Commercial Distribution 🇺🇸 United States

D3

DI: 30014613330592 · Model: 01-0550025 · DIAGNOSTIC HYBRIDS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
D3
Primary DI
30014613330592
Version / Model
01-0550025
Catalog Number
01-0550025
Company Name
DIAGNOSTIC HYBRIDS, INC.
Labeler DUNS
117359612
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-07
Public Version
2
Public Version Date
2023-12-18
Public Version Status
Update
Public Device Record Key
908ea1d9-51d8-45ed-9a63-c623c9b0071d

Device Description

EV MAB CONJUGATE

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
GOE ANTISERA, FLUORESCENT, POLIOVIRUS 1-3

GMDN Terms

Code Name
48243 Multiple-genus respiratory virus antigen IVD, kit, fluorescent immunoassay

Identifiers

Type ID
Primary 30014613330592

Customer Contacts