TourniKwik™
- Primary DI
- 20613994576358
- Brand
- TourniKwik™
- Company
- MEDTRONIC, INC.
- Model
- 79012
- Device description
- TOURNIQUET 79012 TOURNIKWIK 7.5 40PK 17L
- Published
- 2017-07-08
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- false
- OTC
- false
- Sterile
- true
- Single use
- true
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| GDJ | CLAMP, SURGICAL, GENERAL & PLASTIC SURGERY |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| GDJ | Clamp, Surgical, General & Plastic Surgery | General, Plastic Surgery | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 20613994576358 | Primary | GS1 | 0 | |
| 00613994576354 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 20613994576358 | 20613994576358 | ||
| 00613994576354 | 00613994576354 | 613994576354 | 0613994576354 |
GMDN Terms
| Term | Definition |
|---|---|
| Intravascular catheter-snare | A sterile, flexible, end- and/or side-hole tube with a long snaring device (e.g., a wire loop or noose) inserted through its lumen, designed to be introduced into a blood vessel or similar structure to manually retrieve or manipulate a foreign body. It is typically available in two forms: 1) the loop emerges from the distal tip of the catheter while both free ends of the wire emerge from the proximal end; and 2) the end of the wire is attached to the distal end of the catheter while the free end is passed through the lumen to emerge at the proximal end. The wire is usually made of a high-strength, stiff metal [e.g., nickel-titanium alloy (Nitinol)]. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Length | 19.1 | Centimeter |
Sterilization Methods
| Method |
|---|
Contacts
| Phone | |
|---|---|
| +1(800)633-8766 | Corporate.UDI@medtronic.com |
Regulatory Flags
- DUNS number
- 006261481
- Device count
- 40
- DM exempt
- false
- Premarket exempt
- true
- 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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| 00199150080649 | NA | BB12S94R5 | 2026-05-23 | |
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