PITANGUY ABDOMINAL RETRACTOR
- Primary DI
- 00192896043350
- Brand
- PITANGUY ABDOMINAL RETRACTOR
- Company
- SONTEC INSTRUMENTS, INC.
- Model
- 475-924
- Catalog number
- 475-924
- Device description
- PITANGUY ABDOMINAL RETRACTOR LEFT CURVED BLADE
- Published
- 2018-09-18
- 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
- false
Product Codes
| Code | Name |
|---|
| FFO | RETRACTOR, SELF-RETAINING |
| FGN | Retractor, Non-Self-Retaining |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| FFO | Retractor, Self-Retaining | Gastroenterology, Urology | 1 |
| FGN | Retractor, Non-Self-Retaining | Gastroenterology, Urology | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00192896043350 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 00192896043350 | 00192896043350 | 192896043350 | 0192896043350 |
GMDN Terms
| Term | Definition |
|---|
| Externally-anchored laparoscopic retractor | A non-sterile, intraoperative surgical instrument designed for use during laparoscopic procedures to provide hands-free retraction of lower abdominal, urogenital or pelvic structures. It is inserted into the abdominal cavity through a small dedicated incision and manoeuvred into place under direct laparoscopic vision to lift the urogenital structures, and then anchored external to the body to a fixation device typically attached to the operating table. It is typically made of metal (e.g., stainless steel) and is in the form of a rod shaped to form a saddle-shaped hook, and may be available in left and right configurations. This is a reusable device intended to be sterilized prior to use. |
Device Sizes
| Type | Value | Unit |
|---|
| Length | 190 | Millimeter |
Sterilization Methods
| Method |
|---|
| Dry Heat Sterilization;Moist Heat or Steam Sterilization |
Regulatory Flags
- DUNS number
- 040729840
- Device count
- 1
- 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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