NA
- Primary DI
- 04055207000229
- Brand
- NA
- Company
- Richard Wolf GmbH
- Model
- 815032
- Catalog number
- 815.032
- Device description
- HF CONNECTION CABLE MONO L 3M reusable
- Published
- 2016-09-28
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- false
- OTC
- false
- Sterile
- false
- Single use
- false
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | General, Plastic Surgery | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 04055207000229 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04055207000229 | 04055207000229 | 4055207000229 |
GMDN Terms
| Term | Definition |
|---|---|
| Electrical-only medical device connection cable, reusable | A non-patient-contact, insulated, electrical cord with a connector (plug) at both ends designed to transmit electrical power and/or signal (data) between medical devices (e.g., to connect a lead, electrical catheter, handpiece, or monitor to a parent device). It is not intended to connect directly to patient-worn electrodes (i.e., it is not a lead), is not intended to connect to the mains (i.e., not a mains power cable), does not generate any type of power and/or signal, and has no additional non-electrical conducting or processing functionality. This is a reusable device. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Length | 3 | Meter |
Sterilization Methods
| Method |
|---|
| Hydrogen Peroxide;Ethylene Oxide;Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| +497043350 | info@richard-wolf.com |
Regulatory Flags
- DUNS number
- 315304071
- Device count
- 1
- DM exempt
- true
- 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
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
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| 04055207069813 | NA | 892408422 | 892408422 | 2026-01-14 |
| 04055207069820 | NA | 892408425 | 892408425 | 2026-01-14 |
| 04055207069837 | NA | 892408922 | 892408922 | 2026-01-14 |
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| 04055207000328 | NA | 2030105 | 2030.105 | 2023-01-11 |
| 04055207067987 | VERTEBRIS | 892201278 | 892201278 | 2025-11-17 |
| 04055207067994 | VERTEBRIS | 892202007 | 892202007 | 2025-11-17 |
| 04055207068007 | VERTEBRIS | 892202008 | 892202008 | 2025-11-17 |
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