RETRACTOR
- Primary DI
- 00888118020437
- Brand
- RETRACTOR
- Company
- KLS-Martin L.P.
- Model
- 15-079-02-07
- Published
- 2018-09-26
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Related Records
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 |
|---|---|---|---|---|
| 00888118020437 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00888118020437 | 00888118020437 | 888118020437 | 0888118020437 |
GMDN Terms
| Term | Definition |
|---|---|
| Hand-held surgical retractor, reusable | A hand-held, non-self-retaining surgical instrument intended to be used to separate/draw aside the margins of a wound/incision to allow access to tissues/organs during open surgery; it is not dedicated to ophthalmic surgery or small nerve/vessel retraction, but may otherwise be clinically dedicated. It includes a shaped/hooked blade with a handle/holding portion and is available in a wide variety of designs, such as a double- or single-ended blade that may be fenestrated (pronged); deep wound retractors are typically designed with a long, curved blade that may also be intended to retract organs; it may include a light. 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
- 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
Other Devices From This Company
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 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 | |
| 00888118153050 | IXOS | CTM-263-203-01 | 2026-05-25 | |
| 00888118153067 | IXOS | CTM-263-203-02 | 2026-05-25 | |
| 00888118153074 | IXOS | CTM-263-203-03 | 2026-05-25 | |
| 00888118153081 | IXOS | CTM-263-203-04 | 2026-05-25 |
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