Primary Device ID | 07613327067101 |
NIH Device Record Key | a2412810-0305-400b-85b9-956feae16bbd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ACCULIF |
Version Model Number | 800257 |
Catalog Number | 800257 |
Company DUNS | 149183167 |
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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327067101 [Primary] |
MAX | Intervertebral fusion device with bone graft, lumbar |
Steralize Prior To Use | true |
Device Is Sterile | false |
[07613327067101]
Moist Heat or Steam Sterilization
[07613327067101]
Moist Heat or Steam Sterilization
[07613327067101]
Moist Heat or Steam Sterilization
[07613327067101]
Moist Heat or Steam Sterilization
[07613327067101]
Moist Heat or Steam Sterilization
[07613327067101]
Moist Heat or Steam Sterilization
[07613327067101]
Moist Heat or Steam Sterilization
[07613327067101]
Moist Heat or Steam Sterilization
[07613327067101]
Moist Heat or Steam Sterilization
[07613327067101]
Moist Heat or Steam Sterilization
[07613327067101]
Moist Heat or Steam Sterilization
[07613327067101]
Moist Heat or Steam Sterilization
[07613327067101]
Moist Heat or Steam Sterilization
[07613327067101]
Moist Heat or Steam Sterilization
[07613327067101]
Moist Heat or Steam Sterilization
[07613327067101]
Moist Heat or Steam Sterilization
[07613327067101]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-24 |
07613327106046 | PL INSERTION HANDLE INNER SHAFT |
07613327106039 | PL TRIAL |
07613327106022 | TL TRIAL |
07613327106008 | INSTRUMENT TRAY BASE |
07613327105995 | PL TRIAL |
07613327105988 | PL TRIAL |
07613327105971 | PL TRIAL |
07613327105964 | TL TRIAL |
07613327105957 | TL TRIAL |
07613327105940 | TL INSERTION HANDLE |
07613327105933 | PL TRIAL |
07613327105926 | PL INSERTION HANDLE |
07613327105919 | GRAFT INSERTION PUSHER |
07613327105902 | PL TRIAL |
07613327105896 | GRAFT INSERTION CANNULA |
07613327105889 | TL INSERTION HANDLE INNER SHAFT |
07613327105872 | SLAP HAMMER |
07613327105865 | INSERTION HANDLE END CAP |
07613327105858 | INSERTION HANDLE ROTATOR KNOB |
07613327105841 | TL TRIAL |
07613327105834 | TL TRIAL |
07613327105827 | TL TRIAL |
07613327105810 | PREP BLOCK |
07613327105803 | INSTRUMENT TRAY INSERT |
07613327105797 | INSTRUMENT TRAY LID |
07613327068061 | TL CAGE |
07613327068054 | TL CAGE |
07613327068030 | TL CAGE |
07613327067118 | SYRINGE BODY |
07613327067101 | SYRINGE PLUNGER |
37613327067096 | SYRINGE BODY O-RING (GREEN) |
37613327067089 | SYRINGE PLUNGER O-RING (RED) |
07613327067071 | PL Tubing Set |
07613327067064 | TL Tubing Set |
07613327066777 | PL CAGE |
07613327066760 | PL CAGE |
07613327066753 | PL CAGE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ACCULIF 85212265 4106706 Live/Registered |
HOWMEDICA OSTEONICS CORP. 2011-01-06 |