DEKNATEL
- Primary DI
- 34026704426837
- Brand
- DEKNATEL
- Company
- TELEFLEX INCORPORATED
- Model
- IPN026898
- Catalog number
- X-4647M6
- Device description
- STL MF 1 18"X6
- Published
- 2018-07-26
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Product Codes
| Code | Name |
|---|
| GAQ | Suture, nonabsorbable, steel, monofilament and multifilament, sterile |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| GAQ | Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile | General, Plastic Surgery | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 34026704426837 | Package | GS1 | 12 | In Commercial Distribution |
| 04026704426836 | Previous | GS1 | 0 | |
| 14026704426833 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|
| 34026704426837 | 34026704426837 | |
| 04026704426836 | 04026704426836 | 4026704426836 |
| 14026704426833 | 14026704426833 | |
GMDN Terms
| Term | Definition |
|---|
| Metallic suture, monofilament | A sterile, single-strand (monofilament), non-bioabsorbable wire made of metal (e.g., surgical steel, titanium, tantalum) intended to join (approximate) the edges of a soft-tissue wound or incision by stitching (e.g., for abdominal wound closure, intestinal anastomosis, hernia repair), or transosseous (through bone) stitching (e.g., sternal closure); it may include an attached needle intended to be disposed of after single use. It is used primarily in orthopaedic, neurosurgical, and thoracic applications and provides temporary wound support until the wound sufficiently heals to withstand normal stress; it may be retained for permanent support. This is a single-use device. |
Device Sizes
| Type | Value | Unit |
|---|
| Device Size Text, specify | 0 | |
| Length | 45 | Centimeter |
Regulatory Flags
- DUNS number
- 002348191
- 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
- true
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- true
- Sterilization required before use
- false
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