FDA UDI
In Commercial Distribution
🇺🇸 United States
Alinity m
DI: 00884999051096
·
Model: 2
·
ABBOTT MOLECULAR INC.
Product Codes
4
GMDN Terms
1
Identifiers
2
Pkg Device Count
1
Basic Information
- Brand Name
- Alinity m
- Primary DI
- 00884999051096
- Version / Model
- 2
- Catalog Number
- 09N17-03B
- Company Name
- ABBOTT MOLECULAR INC.
- Labeler DUNS
- 878263359
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2023-09-14
- Public Version
- 1
- Public Version Date
- 2023-09-22
- Public Version Status
- New
- Public Device Record Key
- b81e1a03-551d-4ad5-8d38-a46caeabc11c
Device Description
Alinity m STI Application Specification File
Device Characteristics
- Single Use
- No
- 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
- Yes
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- No
- Has Manufacturing Date
- No
- Has Expiration Date
- No
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| LSL | Dna-Reagents, Neisseria | Microbiology | 866.3390 | 2 |
| MKZ | Dna Probe, Nucleic Acid Amplification, Chlamydia | Microbiology | 866.3120 | 1 |
| QEP | Nucleic Acid Detection System For Non-Viral Microorganism(S) Causing Sexually Transmitted Infections | Microbiology | 866.3393 | 2 |
| OUY | Trichomonas Vaginalis Nucleic Acid Amplification Test System | Immunology | 866.3860 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 43472 | Laboratory instrument/analyser application software IVD | An in vitro diagnostic software program intended to be used with an instrument/analyser (e.g., microscope slide digital imaging scanner, immunoassay analyser, real-time PCR machine), or a data management device connected to the instrument/analyser, to: 1) facilitate user-controlled device function [e.g., incubation control]; 2) assist data processing, display, or communication [e.g., image conversion]; and/or 3) produce raw-data-derived qualitative result calculations based on specified criteria [positive or negative assay result]. This software does not use demographic or clinical data to produce a patient score (i.e., it is not interpretive). | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00884999051096 | GS1 | ||||
| Previous | 00884999048669 | GS1 |
Customer Contacts
- Phone
- +1(800) 553-7042
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K222379 | 000 |