3M™
- Primary DI
- 00707387468095
- Brand
- 3M™
- Company
- 3M COMPANY
- Model
- 21174
- Catalog number
- 21174
- Device description
- 21174 SCOTCHPLATE 2 CABLE FOR REM
- Published
- 2016-09-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
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 |
|---|---|---|---|---|
| 00707387468095 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00707387468095 | 00707387468095 | 707387468095 | 0707387468095 |
GMDN Terms#
| Term | Definition |
|---|---|
| Electrosurgical return electrode, single-use, non-sterile | A non-sterile dispersive conductor intended to be fastened to a patient and connected to an electrosurgical/radio-frequency ablation system generator, to allow return of electrical current from the patient to the generator during an electrosurgical procedure. It has a large surface area and is fastened to the patient's body typically where the greatest surface area can be covered in closest proximity to the surgical site. It may or may not include a return cable(s). This is a single-use device. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)228-3957 | 3Mhealthcarecompliance@mmm.com |
Regulatory Flags#
- DUNS number
- 830016148
- Device count
- 1
- Premarket exempt
- true
- Lot or batch
- true
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| 00707387818975 | 3M™ Bair Hugger™ | 55578 | 55578 | 2026-05-15 |
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| 10605861077399 | 3M™ Filtek™ | 4867A2 | 4867A2 | 2026-05-08 |
| 10605861077405 | 3M™ Filtek™ | 4867A3 | 4867A3 | 2026-05-08 |
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