ADMIRAL XTREME
GUDID 08033477052984
Cath ADM070200080 ADM US 07.00L200UL0800
MEDTRONIC, INC.
Peripheral angioplasty balloon catheter, basic Peripheral angioplasty balloon catheter, basic Peripheral angioplasty balloon catheter, basic Peripheral angioplasty balloon catheter, basic Peripheral angioplasty balloon catheter, basic Peripheral angioplasty balloon catheter, basic Peripheral angioplasty balloon catheter, basic Peripheral angioplasty balloon catheter, basic Peripheral angioplasty balloon catheter, basic Peripheral angioplasty balloon catheter, basic Peripheral angioplasty balloon catheter, basic Peripheral angioplasty balloon catheter, basic Peripheral angioplasty balloon catheter, basic| Primary Device ID | 08033477052984 |
| NIH Device Record Key | f8c4f9fe-7f35-4676-bd18-d749ed16194e |
| Commercial Distribution Discontinuation | 2018-10-05 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | ADMIRAL XTREME |
| Version Model Number | ADM070200080 |
| Company DUNS | 006261481 |
| 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 |
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 |
Device Dimensions
| Length | 200 Millimeter |
| Outer Diameter | 7 Millimeter |
| Length | 200 Millimeter |
| Outer Diameter | 7 Millimeter |
| Length | 200 Millimeter |
| Outer Diameter | 7 Millimeter |
| Length | 200 Millimeter |
| Outer Diameter | 7 Millimeter |
| Length | 200 Millimeter |
| Outer Diameter | 7 Millimeter |
| Length | 200 Millimeter |
| Outer Diameter | 7 Millimeter |
| Length | 200 Millimeter |
| Outer Diameter | 7 Millimeter |
| Length | 200 Millimeter |
| Outer Diameter | 7 Millimeter |
| Length | 200 Millimeter |
| Outer Diameter | 7 Millimeter |
| Length | 200 Millimeter |
| Outer Diameter | 7 Millimeter |
| Length | 200 Millimeter |
| Outer Diameter | 7 Millimeter |
| Length | 200 Millimeter |
| Outer Diameter | 7 Millimeter |
| Length | 200 Millimeter |
| Outer Diameter | 7 Millimeter |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *Store at controlled room temperature in a dry place. Do not expose to organic solvents (e.g. alcohol), ionizing radiation or ultraviolet light. |
| Special Storage Condition, Specify | Between 0 and 0 *Store at controlled room temperature in a dry place. Do not expose to organic solvents (e.g. alcohol), ionizing radiation or ultraviolet light. |
| Special Storage Condition, Specify | Between 0 and 0 *Store at controlled room temperature in a dry place. Do not expose to organic solvents (e.g. alcohol), ionizing radiation or ultraviolet light. |
| Special Storage Condition, Specify | Between 0 and 0 *Store at controlled room temperature in a dry place. Do not expose to organic solvents (e.g. alcohol), ionizing radiation or ultraviolet light. |
| Special Storage Condition, Specify | Between 0 and 0 *Store at controlled room temperature in a dry place. Do not expose to organic solvents (e.g. alcohol), ionizing radiation or ultraviolet light. |
| Special Storage Condition, Specify | Between 0 and 0 *Store at controlled room temperature in a dry place. Do not expose to organic solvents (e.g. alcohol), ionizing radiation or ultraviolet light. |
| Special Storage Condition, Specify | Between 0 and 0 *Store at controlled room temperature in a dry place. Do not expose to organic solvents (e.g. alcohol), ionizing radiation or ultraviolet light. |
| Special Storage Condition, Specify | Between 0 and 0 *Store at controlled room temperature in a dry place. Do not expose to organic solvents (e.g. alcohol), ionizing radiation or ultraviolet light. |
| Special Storage Condition, Specify | Between 0 and 0 *Store at controlled room temperature in a dry place. Do not expose to organic solvents (e.g. alcohol), ionizing radiation or ultraviolet light. |
| Special Storage Condition, Specify | Between 0 and 0 *Store at controlled room temperature in a dry place. Do not expose to organic solvents (e.g. alcohol), ionizing radiation or ultraviolet light. |
| Special Storage Condition, Specify | Between 0 and 0 *Store at controlled room temperature in a dry place. Do not expose to organic solvents (e.g. alcohol), ionizing radiation or ultraviolet light. |
| Special Storage Condition, Specify | Between 0 and 0 *Store at controlled room temperature in a dry place. Do not expose to organic solvents (e.g. alcohol), ionizing radiation or ultraviolet light. |
| Special Storage Condition, Specify | Between 0 and 0 *Store at controlled room temperature in a dry place. Do not expose to organic solvents (e.g. alcohol), ionizing radiation or ultraviolet light. |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08033477052984 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K100921
FDA Product Code
| DQY | CATHETER, PERCUTANEOUS |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2020-07-20 |
| Device Publish Date | 2016-04-29 |
On-Brand Devices [ADMIRAL XTREME]
| 08033477058207 | CATH ADM090040130 ADM US 09 00L40 UL1300 |
| 08033477058191 | CATH ADM090040080 ADM US 09 00L40 UL0800 |
| 08033477058184 | CATH ADM090020130 ADM US 09 00L20 UL1300 |
| 08033477058177 | CATH ADM090020080 ADM US 09 00L20 UL0800 |
| 08033477058160 | CATH ADM080040130 ADM US 08 00L40 UL1300 |
| 08033477058153 | CATH ADM080040080 ADM US 08 00L40 UL0800 |
| 08033477058146 | CATH ADM080020130 ADM US 08 00L20 UL1300 |
| 08033477058139 | CATH ADM080020080 ADM US 08 00L20 UL0800 |
| 08033477058122 | CATH ADM070080130 ADM US 07 00L80 UL1300 |
| 08033477058115 | CATH ADM070080080 ADM US 07 00L80 UL0800 |
| 08033477058108 | CATH ADM070060130 ADM US 07 00L60 UL1300 |
| 08033477058092 | CATH ADM070060080 ADM US 07 00L60 UL0800 |
| 08033477058085 | CATH ADM070040130 ADM US 07 00L40 UL1300 |
| 08033477058078 | CATH ADM070040080 ADM US 07 00L40 UL0800 |
| 08033477058061 | CATH ADM070020130 ADM US 07 00L20 UL1300 |
| 08033477058054 | CATH ADM070020080 ADM US 07 00L20 UL0800 |
| 08033477058047 | CATH ADM060120130 ADM US 06 00L120UL1300 |
| 08033477058030 | CATH ADM060120080 ADM US 06 00L120UL0800 |
| 08033477058023 | CATH ADM060080130 ADM US 06 00L80 UL1300 |
| 08033477058016 | CATH ADM060080080 ADM US 06 00L80 UL0800 |
| 08033477058009 | CATH ADM060060130 ADM US 06 00L60 UL1300 |
| 08033477057996 | CATH ADM060060080 ADM US 06 00L60 UL0800 |
| 08033477057989 | CATH ADM060040130 ADM US 06 00L40 UL1300 |
| 08033477057972 | CATH ADM060040080 ADM US 06 00L40 UL0800 |
| 08033477057965 | CATH ADM060020130 ADM US 06 00L20 UL1300 |
| 08033477057958 | CATH ADM060020080 ADM US 06 00L20 UL0800 |
| 08033477057941 | CATH ADM050120130 ADM US 05 00L120UL1300 |
| 08033477057934 | CATH ADM050120080 ADM US 05 00L120UL0800 |
| 08033477057927 | CATH ADM050080130 ADM US 05 00L80 UL1300 |
| 08033477057910 | CATH ADM050080080 ADM US 05 00L80 UL0800 |
| 08033477057903 | CATH ADM050060130 ADM US 05 00L60 UL1300 |
| 08033477057897 | CATH ADM050060080 ADM US 05 00L60 UL0800 |
| 08033477057880 | CATH ADM050040130 ADM US 05 00L40 UL1300 |
| 08033477057873 | CATH ADM050040080 ADM US 05 00L40 UL0800 |
| 08033477057866 | CATH ADM050020130 ADM US 05 00L20 UL1300 |
| 08033477057859 | CATH ADM050020080 ADM US 05 00L20 UL0800 |
| 08033477057842 | CATH ADM040120130 ADM US 04 00L120UL1300 |
| 08033477057835 | CATH ADM040120080 ADM US 04 00L120UL0800 |
| 08033477057828 | CATH ADM040080130 ADM US 04 00L80 UL1300 |
| 08033477057811 | CATH ADM040080080 ADM US 04 00L80 UL0800 |
| 08033477057804 | CATH ADM040060130 ADM US 04 00L60 UL1300 |
| 08033477057798 | CATH ADM040060080 ADM US 04 00L60 UL0800 |
| 08033477057781 | CATH ADM040040130 ADM US 04 00L40 UL1300 |
| 08033477057774 | CATH ADM040040080 ADM US 04 00L40 UL0800 |
| 08033477057767 | CATH ADM040020130 ADM US 04 00L20 UL1300 |
| 08033477057750 | CATH ADM040020080 ADM US 04 00L20 UL0800 |
| 08033477057743 | CATH ADM030120130 ADM US 03 00L120UL1300 |
| 08033477057736 | CATH ADM030120080 ADM US 03 00L120UL0800 |
| 08033477057729 | CATH ADM030080130 ADM US 03 00L80 UL1300 |
| 08033477057712 | CATH ADM030080080 ADM US 03 00L80 UL0800 |
Trademark Results [ADMIRAL XTREME]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ADMIRAL XTREME 79024620 not registered Dead/Abandoned |
INVATEC S.P.A. 2006-04-06 |
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