FDA UDI
In Commercial Distribution
🇺🇸 United States
Phospholin ES w/ Calcium Chloride
DI: 10859394006016
·
Model: 21-410
·
R 2 DIAGNOSTICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5
Basic Information
- Brand Name
- Phospholin ES w/ Calcium Chloride
- Primary DI
- 10859394006016
- Version / Model
- 21-410
- Catalog Number
- 21-410
- Company Name
- R 2 DIAGNOSTICS, INC.
- Labeler DUNS
- 956610125
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 5
- Record Status
- Published
- Publish Date
- 2016-11-15
- Public Version
- 3
- Public Version Date
- 2018-07-06
- Public Version Status
- Update
- Public Device Record Key
- ae9c351f-f3f7-48ca-83e9-9a89bab556bf
Device Description
APTT reagent 5 x 10 ml with 5 Calcium Chloride
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- No
- 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
- 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 |
|---|---|---|---|---|
| GGW | Test, Time, Partial Thromboplastin | Hematology | 864.7925 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 55982 | Activated partial thromboplastin time (APTT) 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 quantitative measurement of the activated partial thromboplastin time (APTT) of a clinical specimen. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 10859394006016 | GS1 | ||||
| Unit of Use | 00859394006019 | GS1 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K033471 | 000 |