FDA UDI
In Commercial Distribution
🇺🇸 United States
LupoTek Correctin VL
DI: 10859394006115
·
Model: 86-201
·
R 2 DIAGNOSTICS, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
10
Basic Information
- Brand Name
- LupoTek Correctin VL
- Primary DI
- 10859394006115
- Version / Model
- 86-201
- Catalog Number
- 86-201
- Company Name
- R 2 DIAGNOSTICS, INC.
- Labeler DUNS
- 956610125
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 10
- 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
- f0a42414-4ae5-4460-bc89-86d341bf5c27
Device Description
Venom Confirmatory test for LA 10 x 1 ml
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 |
|---|---|---|---|---|
| GIR | Reagent, Russel Viper Venom | Hematology | 864.8950 | 1 |
| GGC | Control, Plasma, Abnormal | Hematology | 864.5425 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 56202 | Lupus anticoagulant marker IVD, kit, clotting | A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of one or multiple Lupus anticoagulant markers in a clinical specimen, using a clotting method. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 10859394006115 | GS1 | ||||
| Unit of Use | 00859394006118 | GS1 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K083878 | 000 |