Primary Device ID | 00889024205185 |
NIH Device Record Key | dea5674d-36c8-4bad-afb9-6ba747deabdf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AccuPort Zone Delivery 8 Ga x 150mm Drill Length |
Version Model Number | 308.064 |
Catalog Number | 308.064 |
Company DUNS | 078836317 |
Company Name | ZIMMER KNEE CREATIONS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 484-887-8902 |
KC.Customerservice@zimmerbiomet.com |
Needle Gauge | 8 Gauge |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024205185 [Primary] |
FGY | Cannula, Injection |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-02-07 |
Device Publish Date | 2016-05-18 |
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