FDA UDI In Commercial Distribution 🇺🇸 United States

APTIMA

DI: 15420045505490 · Model: TRICHOMONAS VAGINALIS, 250T, IVD (REF)V2 · Hologic, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
APTIMA
Primary DI
15420045505490
Version / Model
TRICHOMONAS VAGINALIS, 250T, IVD (REF)V2
Catalog Number
303163; 303164
Company Name
Hologic, Inc.
Labeler DUNS
050579217
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-03-23
Public Version
4
Public Version Date
2020-12-21
Public Version Status
Update
Public Device Record Key
dfa2fe1c-8253-40b4-8860-0a5ea47344eb

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
Yes
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
OUY Trichomonas vaginalis nucleic acid amplification test system

GMDN Terms

Code Name
50409 Multiple-type sexually transmitted pathogen nucleic acid IVD, kit, nucleic acid technique (NAT)

Identifiers

Type ID
Primary 15420045505490

Premarket Submissions

Submission Number Supplement Number
K122062 000