Technicuff
- Primary DI
- 00819980010097
- Brand
- Technicuff
- Company
- TECHNICUFF CORP.
- Model
- UA-1745
- Device description
- Adult Blood Pressure Cuff 50 each
- Published
- 2016-09-14
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- false
- OTC
- false
- Sterile
- false
- Single use
- false
Product Codes
| Code | Name |
|---|
| DXQ | Blood Pressure Cuff |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| DXQ | Blood Pressure Cuff | Cardiovascular | 2 |
Premarket Details
| Submission | Supplement | Device | Applicant | Decision date | Product code |
|---|
| K942259 | 000 | TECHNICUFF | Technicuff Corp. | 1994-09-06 | DXQ |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00819980010097 | Primary | GS1 | 0 | |
GMDN Terms
| Term | Definition |
|---|
| Patient monitoring system module, blood pressure, noninvasive | A small unit dedicated to the measurement of noninvasive blood pressure (indirect method) obtained through a standard sphygmomanometer cuff placed on the arm or leg. It is designed to operate as part of a patient monitoring system enhancing the function of this system (the parent device). The module automatically plugs into the parent device when the user places it into a standardized slot in the parent device or a connected module rack. The parent device operates as a mainframe computer displaying the blood pressure parameter/information measured and provided by this module. |
Regulatory Flags
- DUNS number
- 148745805
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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