BLADE
- Primary DI
- 00888118022523
- Brand
- BLADE
- Company
- KLS-Martin L.P.
- Model
- 15-859-01-07
- Device description
- RETRACTOR, CENTRAL, BALFOUR, FOR 15-858-00
- Published
- 2018-09-26
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| GAD | RETRACTOR |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| GAD | Retractor | General, Plastic Surgery | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00888118022523 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00888118022523 | 00888118022523 | 888118022523 | 0888118022523 |
GMDN Terms#
| Term | Definition |
|---|---|
| Surgical retractor/retraction system blade, reusable | A distal component of a surgical retraction system, surgical retractor, and/or surgical instrument assist arm system designed to function as a parting edge to separate the margins of a wound/incision during an open surgical procedure. It is intended to be attached to the frame (e.g., mounting ring/bar) of a surgical retraction system, or may be fixed onto a retractor handle; it does not include a handle. It is sometimes referred to as a variable or vario retractor blade when assembled with a separate retractor handle because it is available in a variety of lengths and sizes. It is made of high-grade stainless steel. This is a reusable device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(904)641-7746 | KLS-UDI-Info@klsmartin.com |
Regulatory Flags#
- DUNS number
- 826499238
- Device count
- 1
- Premarket exempt
- true
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00888118019547 | FORCEPS | 13-451-20-07 | 2018-09-26 | |
| 00888118069085 | PROBE | 43-736-06-07 | 2018-09-26 | |
| 00888118143037 | LEVEL ONE THORACIC, STERILE | 24-015-39-71 | 2024-10-08 | |
| 00888118143044 | LEVEL ONE THORACIC, STERILE | 24-015-49-71 | 2024-10-08 | |
| 00888118131782 | LEVEL ONE EXTREMITY | 26-066-60-09 | 2026-05-25 | |
| 00888118131799 | LEVEL ONE EXTREMITY | 26-066-70-09 | 2026-05-25 | |
| 00888118144928 | LEVEL ONE EXTREMITY | 26-950-40-07 | 2026-05-25 | |
| 00888118145284 | PURE PECTUS | 24-070-60-09 | 2026-05-25 | |
| 00888118145291 | PURE PECTUS | 24-070-62-09 | 2026-05-25 | |
| 00888118150240 | PURE PECTUS | CTM-241-100-01 | 2026-05-25 | |
| 00888118150257 | PURE PECTUS | CTM-241-101-01 | 2026-05-25 | |
| 00888118150264 | PURE PECTUS | CTM-241-200-01 | 2026-05-25 | |
| 00888118150448 | IXOS | CTM-263-100-01 | 2026-05-25 | |
| 00888118150455 | IXOS | CTM-263-101-01 | 2026-05-25 | |
| 00888118150462 | IXOS | CTM-263-202-01 | 2026-05-25 | |
| 00888118150479 | IXOS | CTM-263-202-02 | 2026-05-25 | |
| 00888118150486 | IXOS | CTM-263-202-03 | 2026-05-25 | |
| 00888118150493 | IXOS | CTM-263-202-04 | 2026-05-25 | |
| 00888118150646 | IPS | 60-011-42-09-LP | 2026-05-25 | |
| 00888118153029 | L1 STERNAL | CTM-242-302-01 | 2026-05-25 |
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