CODMAN®
- Primary DI
- 10381780513919
- Brand
- CODMAN®
- Company
- INTEGRA LIFESCIENCES PRODUCTION CORPORATION
- Model
- 301536
- Catalog number
- 30-1536
- Device description
- CODMAN® Bipolar Cord
- Published
- 2020-02-28
- 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 |
|---|---|
| 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 |
|---|---|---|---|---|
| 10886704006107 | Previous | GS1 | 0 | |
| 10381780513919 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10886704006107 | 10886704006107 |
| 10381780513919 | 10381780513919 |
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. |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | Waste Electrical and Electronic Equipment |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)654-2873 | custsvcnj@integralife.com |
Regulatory Flags#
- DUNS number
- 081277700
- Device count
- 1
- Premarket exempt
- true
- Lot or batch
- true
- Manufacturing date on label
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10381780024507 | Integra® Jarit® | 100539 | 100-539 | 2018-01-22 |
| 10381780024514 | Integra® Jarit® | 100540 | 100-540 | 2018-01-22 |
| 10381780031901 | Integra® Miltex® | 27-202 | 27-202 | 2015-09-22 |
| 10381780031918 | Integra® Miltex® | 27-204 | 27-204 | 2015-09-22 |
| 10381780031925 | Integra® Miltex® | 27-206 | 27-206 | 2015-09-22 |
| 10381780031932 | Integra® Miltex® | 27-208 | 27-208 | 2015-09-22 |
| 10381780031949 | Integra® Miltex® | 27-210 | 27-210 | 2015-09-22 |
| 10381780031956 | Integra® Miltex® | 27-212 | 27-212 | 2015-09-22 |
| 10381780063865 | Integra® Miltex® | 4-515C | 4-515C | 2018-02-15 |
| 10381780063872 | Integra® Miltex® | 4-522 | 4-522 | 2018-02-15 |
| 10381780063896 | Integra® Miltex® | 4611 | 4611 | 2018-02-15 |
| 10381780063902 | Integra® Miltex® | 4615 | 4615 | 2018-02-15 |
| 10381780064206 | Integra® Miltex® | 33-38 | 33-38 | 2018-02-14 |
| 10381780128779 | Integra® Miltex® | 30-1740 | 30-1740 | 2016-08-03 |
| 10381780133810 | Integra® Jarit® | 320437 | 320-437 | 2016-08-12 |
| 10381780134503 | Integra® Jarit® | 653101 | 653101 | 2018-01-15 |
| 10381780136408 | Integra® Jarit® | X37254 | X37254 | 2016-08-14 |
| 10381780142874 | Integra® Jarit® | 230250 | 230-250 | 2016-08-14 |
| 10381780143048 | Integra® Jarit® | 320195 | 320-195 | 2016-08-14 |
| 10381780143055 | Integra® Jarit® | 320196 | 320-196 | 2016-08-14 |
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