FDA UDI
In Commercial Distribution
🇺🇸 United States
APTIMA
DI: 15420045509153
·
Model: BX 2 (RT) M GEN, 100T, AS, IVD
·
Hologic, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- APTIMA
- Primary DI
- 15420045509153
- Version / Model
- BX 2 (RT) M GEN, 100T, AS, IVD
- Catalog Number
- PRD-03374 / PRD-03919
- Company Name
- Hologic, Inc.
- Labeler DUNS
- 153623137
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2019-01-25
- Public Version
- 2
- Public Version Date
- 2022-10-05
- Public Version Status
- Update
- Public Device Record Key
- ced65bd2-8d4a-4506-b624-2291c2f65eee
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 | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| QEP | Mycoplasma Genitalium Nucleic Acid Detection System | Microbiology | 866.3393 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 47325 | Mycoplasma genitalium nucleic acid IVD, reagent | A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of nucleic acid from Mycoplasma genitalium bacteria in a clinical specimen. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 15420045509153 | GS1 |