IZDS 451102-5
GUDID 04546540675828
Connecting Cable
Stryker Corporation
Vascular implant detacher, single-use, sterile| Primary Device ID | 04546540675828 |
| NIH Device Record Key | d88b1fc3-9ce6-4015-83aa-050a35734348 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | IZDS |
| Version Model Number | M00345110250 |
| Catalog Number | 451102-5 |
| Company DUNS | 042405446 |
| Company Name | Stryker Corporation |
| 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 | true |
| 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
Device Dimensions
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
| Length | 180 Centimeter |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04546540675828 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K092666
FDA Product Code
| HCG | DEVICE, NEUROVASCULAR EMBOLIZATION |
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 | 2015-09-21 |
Devices Manufactured by Stryker Corporation
| 07613327272246 - ARIA | 2025-09-25 IMPLANT IMPACTOR |
| 37613327405317 - SurgiCount Safety-Sponge | 2025-09-16 Laparotomy Sponge |
| 07613327262209 - XIA | 2025-09-11 FRENCH BENDER |
| 07613327262216 - XIA | 2025-09-11 SPREADER |
| 07613327262254 - XIA | 2025-09-11 COMPRESSOR |
| 07613327262261 - XIA | 2025-09-11 BLUNT PROBE |
| 07613327262292 - XIA | 2025-09-11 TORQUE WRENCH |
| 07613327262414 - XIA | 2025-09-11 STANDARD T-HANDLE |
Trademark Results [IZDS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 IZDS 77627238 3908508 Live/Registered |
STRYKER CORPORATION 2008-12-05 |
IZDS 77627238 3908508 Live/Registered |
STRYKER EUROPEAN HOLDINGS I, LLC 2008-12-05 |
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