Primary Device ID | 10884389810194 |
NIH Device Record Key | 9111bec7-a6cf-44d6-a7a7-94b6c645c758 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MAXORB |
Version Model Number | ES - Reinforced Alginate |
Catalog Number | MSC7918EP |
Company DUNS | 770434090 |
Company Name | ADVANCED MEDICAL SOLUTIONS LIMITED |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10884389810194 [Primary] |
NAC | Dressing, Wound, Hydrophilic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-12-15 |
Device Publish Date | 2022-12-07 |
10884389810194 | 14-21BP Reinforced CMC/ Alginate Ribbon |
10884389124055 | 14-24AP Silver Alginate II |
10080196297122 | 14-24AP Silver Alginate II |
10080196297115 | 14-24AP Silver Alginate II |
10080196297108 | 14-24AP Silver Alginate II |
10080196297092 | 14-24AP Silver Alginate II |
10080196296835 | 14-21BP |
10080196296828 | 14-21BP |
10080196293506 | 14-21BP |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MAXORB 75242408 2241864 Live/Registered |
Medline Industries, Inc. 1997-02-18 |
MAXORB 74125385 not registered Dead/Abandoned |
TABB TEXTILE SYSTEMS, INC. 1990-12-21 |
MAXORB 73327743 1251068 Dead/Cancelled |
MPD Technology Corporation 1981-09-14 |
MAXORB 73191883 1184433 Dead/Cancelled |
MPD Technology Corporation 1978-11-03 |