FDA UDI In Commercial Distribution 🇺🇸 United States

APTIMA

DI: 15420045512900 · Model: KIT,APTIMA COMBO 2,100T,RT,CEIVD-UPDATED · Hologic, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
APTIMA
Primary DI
15420045512900
Version / Model
KIT,APTIMA COMBO 2,100T,RT,CEIVD-UPDATED
Catalog Number
PRD-05576
Company Name
Hologic, Inc.
Labeler DUNS
050579217
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-16
Public Version
2
Public Version Date
2020-12-21
Public Version Status
Update
Public Device Record Key
9545dd3b-30a0-4ba0-9e36-cd4e9aa55d24

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
MKZ DNA PROBE, NUCLEIC ACID AMPLIFICATION, CHLAMYDIA
QEP Nucleic acid detection system for non-viral microorganism(s) causing sexually transmitted infections
LSL DNA-REAGENTS, NEISSERIA

GMDN Terms

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

Identifiers

Type ID
Primary 15420045512900

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius