Primary Device ID | 07613252193951 |
NIH Device Record Key | 8173372f-172b-444d-ac2c-e461848c291b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Neuroform Stabilizer |
Version Model Number | M003SNF3STA0 |
Catalog Number | M003SNF3STA0 |
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 |
Phone | +1(855)916-3876 |
NVCustomerService@stryker.com | |
Phone | +1(855)916-3876 |
NVCustomerService@stryker.com | |
Phone | +1(855)916-3876 |
NVCustomerService@stryker.com | |
Phone | +1(855)916-3876 |
NVCustomerService@stryker.com | |
Phone | +1(855)916-3876 |
NVCustomerService@stryker.com | |
Phone | +1(855)916-3876 |
NVCustomerService@stryker.com | |
Phone | +1(855)916-3876 |
NVCustomerService@stryker.com | |
Phone | +1(855)916-3876 |
NVCustomerService@stryker.com | |
Phone | +1(855)916-3876 |
NVCustomerService@stryker.com | |
Phone | +1(855)916-3876 |
NVCustomerService@stryker.com | |
Phone | +1(855)916-3876 |
NVCustomerService@stryker.com | |
Phone | +1(855)916-3876 |
NVCustomerService@stryker.com | |
Phone | +1(855)916-3876 |
NVCustomerService@stryker.com | |
Phone | +1(855)916-3876 |
NVCustomerService@stryker.com | |
Phone | +1(855)916-3876 |
NVCustomerService@stryker.com |
Length | 152 Centimeter |
Length | 152 Centimeter |
Lumen/Inner Diameter | 0.016 Inch |
Length | 152 Centimeter |
Lumen/Inner Diameter | 0.016 Inch |
Length | 152 Centimeter |
Lumen/Inner Diameter | 0.016 Inch |
Length | 152 Centimeter |
Lumen/Inner Diameter | 0.016 Inch |
Length | 152 Centimeter |
Lumen/Inner Diameter | 0.016 Inch |
Length | 152 Centimeter |
Lumen/Inner Diameter | 0.016 Inch |
Length | 152 Centimeter |
Lumen/Inner Diameter | 0.016 Inch |
Length | 152 Centimeter |
Lumen/Inner Diameter | 0.016 Inch |
Length | 152 Centimeter |
Lumen/Inner Diameter | 0.016 Inch |
Length | 152 Centimeter |
Lumen/Inner Diameter | 0.016 Inch |
Length | 152 Centimeter |
Lumen/Inner Diameter | 0.016 Inch |
Length | 152 Centimeter |
Lumen/Inner Diameter | 0.016 Inch |
Length | 152 Centimeter |
Lumen/Inner Diameter | 0.016 Inch |
Length | 152 Centimeter |
Lumen/Inner Diameter | 0.016 Inch |
Length | 152 Centimeter |
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 Issuing Agency | Device ID |
---|---|
GS1 | 07613252193951 [Primary] |
NJE | intracranial neurovascular stent |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2016-05-02 |
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07613327648522 - Surpass Elite | 2025-03-17 Flow Diverter System |
07613327648539 - Surpass Elite | 2025-03-17 Flow Diverter System |
07613327648546 - Surpass Elite | 2025-03-17 Flow Diverter System |
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