Vectris™ SureScan®
GUDID 00643169109384
LEAD 977A275 MRICS COMPACT
MEDTRONIC, INC.
Neural-tissue electrical stimulation lead Neural-tissue electrical stimulation lead Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection| Primary Device ID | 00643169109384 |
| NIH Device Record Key | 7d17d84b-b98f-4259-815b-58af1afe0c65 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vectris™ SureScan® |
| Version Model Number | 977A275 |
| Company DUNS | 796986144 |
| Company Name | MEDTRONIC, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
Device Dimensions
| Length | 75 Centimeter |
| Length | 75 Centimeter |
| Length | 75 Centimeter |
| Length | 75 Centimeter |
| Length | 75 Centimeter |
| Length | 75 Centimeter |
| Length | 75 Centimeter |
| Length | 75 Centimeter |
| Length | 75 Centimeter |
| Length | 75 Centimeter |
| Length | 75 Centimeter |
| Length | 75 Centimeter |
| Length | 75 Centimeter |
| Length | 75 Centimeter |
| Length | 75 Centimeter |
| Length | 75 Centimeter |
| Length | 75 Centimeter |
| Length | 75 Centimeter |
Operating and Storage Conditions
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
| Handling Environment Temperature | Between -30 Degrees Fahrenheit and 135 Degrees Fahrenheit |
| Handling Environment Temperature | Between -34 Degrees Celsius and 57 Degrees Celsius |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00643169109384 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Approval: P840001
FDA Product Code
| LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2014-09-23 |
On-Brand Devices [Vectris™ SureScan®]
| 00643169109421 | LEAD 977A160 MRICS SUBCOMPACT |
| 00643169109414 | LEAD 977A175 MRICS SUBCOMPACT |
| 00643169109407 | LEAD 977A190 MRICS SUBCOMPACT |
| 00643169109391 | LEAD 977A260 MRICS COMPACT |
| 00643169109384 | LEAD 977A275 MRICS COMPACT |
| 00643169109377 | LEAD 977A290 MRICS COMPACT |
| 00763000006549 | LEAD 977A290 VECTRIS MRICS SUBCOMPACT |
| 00763000006525 | LEAD 977A275 VECTRIS MRICS SUBCOMPACT |
| 00763000006501 | LEAD 977A260 VECTRIS MRICS SUBCOMPACT |
| 00763000006488 | LEAD 977A190 VECTRIS MRICS SUBCOMPACT |
| 00763000006464 | LEAD 977A175 VECTRIS MRICS SUBCOMPACT |
| 00763000006440 | LEAD 977A160 VECTRIS MRICS SUBCOMPACT |
| 00763000324292 | LEAD 977A290 VECTRIS MRICS SUBCOMPACT |
| 00763000324285 | LEAD 977A275 VECTRIS MRICS SUBCOMPACT |
| 00763000324278 | LEAD 977A260 VECTRIS MRICS SUBCOMPACT |
| 00763000324261 | LEAD 977A190 VECTRIS MRICS SUBCOMPACT |
| 00763000324254 | LEAD 977A175 VECTRIS MRICS SUBCOMPACT |
| 00763000324247 | LEAD 977A160 VECTRIS MRICS SUBCOMPACT |
Trademark Results [Vectris]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VECTRIS 85009043 4324744 Live/Registered |
Medtronic, Inc. 2010-04-08 |
 VECTRIS 77185608 not registered Dead/Abandoned |
Vectris Group Inc. 2007-05-21 |
 VECTRIS 75899678 not registered Dead/Abandoned |
Pronto Aircraft, Corporation 2000-01-20 |
 VECTRIS 75878705 not registered Dead/Abandoned |
Vectris Communications 1999-12-23 |
 VECTRIS 75175558 2166478 Dead/Cancelled |
Ivoclar Vivadent, Inc. 1996-10-01 |
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