Primary Device ID | 00613994571922 |
NIH Device Record Key | 95a5de31-2cc6-4e53-b228-eb0ea78e35e4 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 3550-05 |
Company DUNS | 796986144 |
Company Name | MEDTRONIC, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00613994571922 [Primary] |
GZB | STIMULATOR, SPINAL-CORD, IMPLANTED (PAIN RELIEF) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2014-09-23 |
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00763000582906 - Valve Handle 7420 | 2025-03-03 HANDLE 7420 VLV HNDLE 234MM CEM GLOBAL |
00763000911089 - NA | 2025-03-03 FOOT SWITCH NITRONFS GLOBAL |
20763000954363 - N/A | 2025-03-03 PATCH AFR-00007 LOCATION REF 4PK US |
20763000999197 - NA | 2025-03-03 CUSTOM PACK BB2N27R2 5PK CARDIO LN |
20763000999753 - NA | 2025-03-03 CUSTOM PACK 12M79R 10PK TTS |
20763000999210 - NA | 2025-02-28 CUSTOM PACK BB12D77R2 5PK HEAD PACK |
20763000999234 - NA | 2025-02-28 CUSTOM PACK BB12D89R1 5PK HEAD ACC PACK |