Primary Device ID | 05060459970052 |
NIH Device Record Key | 92115a9d-93ca-46dc-8490-df9936f222cf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Hyalgan |
Version Model Number | None |
Company DUNS | 220744126 |
Company Name | ALLY MEDICAL SUPPLIES LTD |
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 | 516-206-1003 |
jeff@allymedicalsupplies.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05060459970052 [Primary] |
MOZ | Acid, Hyaluronic, Intraarticular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-10-23 |
5060459970014 - Synvisc | 2018-07-06 |
05060459970021 - Synvisc One | 2018-07-06 |
05060459970038 - Orthovisc | 2018-07-06 |
05060459970045 - Euflexxa | 2018-07-06 |
05060459970052 - Hyalgan | 2018-07-06 |
05060459970052 - Hyalgan | 2018-07-06 |
05060459970090 - Monovisc | 2018-07-06 |
05060459970120 - Supartz | 2018-07-06 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HYALGAN 79202959 5388830 Live/Registered |
Fidia Farmaceutici S.p.A. 2016-07-19 |
HYALGAN 73585251 1420772 Live/Registered |
FIDIA S.P.A. 1986-02-28 |