Primary Device ID | 07613327052367 |
NIH Device Record Key | 8cc78ae0-8e57-4fb3-bb53-80f032f10771 |
Commercial Distribution Discontinuation | 2020-03-26 |
Commercial Distribution Status | Not in Commercial Distribution |
Version Model Number | 0250080174 |
Catalog Number | 0250-080-174 |
Company DUNS | 187502109 |
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 | false |
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 |
Phone | +1(866)624-4422 |
xx@xx.xx |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327052367 [Primary] |
GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES |
Steralize Prior To Use | true |
Device Is Sterile | false |
[07613327052367]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2020-03-26 |
Device Publish Date | 2016-09-23 |
07613327627664 - KNOTILUS+ | 2024-03-15 2.9X12.5MM KNOTILUS+ HIP ANCHOR - PEEK |
07613327627701 - KNOTILUS+ | 2024-03-15 2.4X8.9MM KNOTILUS+ HIP ANCHOR - PEEK |
07613327623796 - KNOTILUS+ | 2024-03-13 2.4X8.9MM DRILL, HIP |
07613327623833 - KNOTILUS+ | 2024-03-13 2.4X8.9MM DRILL, HARD BONE, HIP |
07613327634686 - Iconix | 2024-03-12 Iconix DC Guide for 1.4mm anchor |
07613327634693 - Iconix | 2024-03-12 |
07613327616675 - SPY | 2024-03-06 |
07613327616682 - SPY | 2024-03-06 |