Primary Device ID | 07332551227364 |
NIH Device Record Key | 2b75df99-f2a7-4a9e-8b8f-08389677f5de |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Melgisorb |
Version Model Number | Ag Alginate |
Catalog Number | 255050 |
Company DUNS | 770434090 |
Company Name | ADVANCED MEDICAL SOLUTIONS LIMITED |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | true |
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 | 07332551227364 [Primary] |
FRO | Dressing, Wound, Drug |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2023-10-30 |
Device Publish Date | 2022-12-08 |
07332551992040 | 14-24AP Silver Alginate II |
07332551242831 | 14-24AP Silver Alginate II |
07332551227364 | 14-24AP Silver Alginate II |
07332551227357 | 14-24AP Silver Alginate II |
07332551227340 | 14-24AP Silver Alginate II |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MELGISORB 75543934 2450437 Live/Registered |
Mölnlycke Health Care AB 1998-08-27 |