| Primary Device ID | 00643169669024 |
| NIH Device Record Key | e3a49cc0-f94a-48f8-9109-40e0f4350c56 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | URCHIN™ |
| Version Model Number | 29700 |
| Company DUNS | 006261481 |
| Company Name | MEDTRONIC, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| OTC Over-The-Counter | false |
| 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 | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00643169669024 [Primary] |
| MWS | stabilizer,heart |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-07-08 |
| 00763000763152 - NA | 2025-10-07 SW APP P7A2C11 ALTAVIVA CLINICIAN |
| 00763000763817 - NA | 2025-10-07 SW APP P7A2P11 ALTAVIVA PATIENT |
| 00763000929367 - Altaviva™ | 2025-10-07 KIT P7K2C001 ALTAVIVA CLINICIAN |
| 00763000935627 - Altaviva™ | 2025-10-07 KIT P7K2P001 ALTAVIVA PATIENTA^ |
| 00763000936433 - Altaviva™ | 2025-10-07 INS P7850N ALTAVIVA NEUROSTIMULATOR RC |
| 00763000936440 - NA | 2025-10-07 ACCESSORY P71001 POCKET DISSECTOR |
| 00199150050161 - NA | 2025-09-29 CUSTOM PACK HLO BB12D44R4 PUMP PK |
| 00199150050178 - NA | 2025-09-29 CUSTOM PACK BB4W67R26 EVL ADULT E |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() URCHIN 98267396 not registered Live/Pending |
Spacecurve KK 2023-11-13 |
![]() URCHIN 90775757 not registered Live/Pending |
Gong Minzhi 2021-06-15 |
![]() URCHIN 88288810 not registered Live/Pending |
Eiser, Erik 2019-02-04 |
![]() URCHIN 87959751 5661232 Live/Registered |
Zhisheng (Shen zhen) Industrial Co.,Ltd. 2018-06-13 |
![]() URCHIN 86020386 4466582 Live/Registered |
DEI Headquarters, Inc. 2013-07-25 |
![]() URCHIN 79012269 3136015 Dead/Cancelled |
The Entity Australia Pty Limited 2004-11-18 |
![]() URCHIN 78883518 3516511 Dead/Cancelled |
Advanced Engineering Solutions Ltd 2006-05-15 |
![]() URCHIN 78169097 2785094 Dead/Cancelled |
Medtronic, Inc. 2002-09-30 |
![]() URCHIN 77231662 3372779 Dead/Cancelled |
Google Inc. 2007-07-17 |
![]() URCHIN 75749864 2348703 Dead/Cancelled |
Quantified Systems, Inc. 1999-07-14 |
![]() URCHIN 75179347 2071994 Dead/Cancelled |
LARK INTERNATIONAL APPAREL, LTD. 1996-09-30 |