FDA UDI
In Commercial Distribution
🇺🇸 United States
Disposable High Pressure Syringe
DI: 06970286900100
·
Model: SMR302
·
Union Medical Shenzhen Co.,LTD.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1
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Basic Information
- Brand Name
- Disposable High Pressure Syringe
- Primary DI
- 06970286900100
- Version / Model
- SMR302
- Company Name
- Union Medical Shenzhen Co.,LTD.
- Labeler DUNS
- 544445008
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2018-12-26
- Public Version
- 2
- Public Version Date
- 2020-11-26
- Public Version Status
- Update
- Public Device Record Key
- 4df6570f-2f2e-4a4a-a93f-74922b214bfd
Device Characteristics
- Single Use
- Yes
- 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
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- Yes
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| DXT | Injector And Syringe, Angiographic | Cardiovascular | 870.1650 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 15286 | Angiographic syringe | A sterile, manually-operated device consisting of a barrel (cylinder) with plunger intended to be used for the administration of a contrast medium into the heart, great vessels, and coronary arteries to study the heart and vessels under x-ray photography. It may in addition be intended for introduction of other fluids (e.g., saline). It is not intended to be used with a contrast medium injection system. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 56970286900105 | GS1 | 50 | In Commercial Distribution | ||
| Primary | 06970286900100 | GS1 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K170279 | 000 |