GAP ENDO-EXO MEDULLARY SYSTEM
- Primary DI
- 07540194011879
- Brand
- GAP ENDO-EXO MEDULLARY SYSTEM
- Company
- Pega Medical Inc
- Model
- GAP-KWG020-PKG6
- Catalog number
- GAP-KWG020-PKG6
- Device description
- GAP GUIDE WIRE Ø2.0mm - PKG OF 6
- Published
- 2020-08-12
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- true
Product Codes
| Code | Name |
|---|
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| LXH | Orthopedic Manual Surgical Instrument | Orthopedic | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 07540194010070 | Primary | GS1 | 0 | |
| 07540194011879 | Unit of Use | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|
| 07540194010070 | 07540194010070 | 7540194010070 |
| 07540194011879 | 07540194011879 | 7540194011879 |
GMDN Terms
| Term | Definition |
|---|
| Bone nail guidewire, reusable | A long, thin, metal rod designed to guide intramedullary canal devices for performing the implantation of an intramedullary nail to treat damaged bone. The rod is usually manually inserted into the canal to typically guide a surgical instrument (e.g., a reamer) and the implantable nail. This device is made of metal [e.g., high-grade stainless steel, titanium (Ti)] and is available in a variety of sizes, lengths, and designs (e.g., round-tip, trocar-tip, or flexible-tip). It may be used in femoral, tibial, humeral or supracondylar intramedullary canals. This is a reusable device. |
Device Sizes
| Type | Value | Unit |
|---|
| Length | 457.2 | Millimeter |
| Outer Diameter | 2 | Millimeter |
Storage And Handling
| Type | Low | High | Condition |
|---|
| Special Storage Condition, Specify | 0 | 0 | keep at room temperature |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags
- DUNS number
- 257315713
- Device count
- 6
- 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
- true
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