| Primary Device ID | 15032749039166 |
| NIH Device Record Key | 5b27fcad-d527-4051-8f3a-afb7cb2229ea |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Actibride™ |
| Version Model Number | Debridement Pad |
| Catalog Number | 9039169 |
| 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 | 15032749039166 [Primary] |
| NAB | Gauze / Sponge,Nonresorbable For External Use |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-09-09 |
| Device Publish Date | 2024-08-30 |
| 15032749039166 - Actibride™ | 2024-09-09ActivHeal® Actibride™ Debridement Pad 11cmx18cm |
| 15032749039166 - Actibride™ | 2024-09-09 ActivHeal® Actibride™ Debridement Pad 11cmx18cm |
| 15032749040605 - RAPONICEL™ | 2024-05-08 ACTIVHEAL® RAPONICEL™ ULTRA 5x5CM |
| 15032749040612 - RAPONICEL™ | 2024-05-08 ACTIVHEAL® RAPONICEL™ ULTRA 10X10CM |
| 15032749040629 - RAPONICEL™ | 2024-05-08 ACTIVHEAL® RAPONICEL™ ULTRA 10X12CM |
| 15032749040636 - RAPONICEL™ | 2024-05-08 ACTIVHEAL® RAPONICEL™ ULTRA 15X15CM |
| 15032749040643 - RAPONICEL™ | 2024-05-08 ACTIVHEAL® RAPONICEL™ ULTRA 20X30CM |
| 15032749040650 - RAPONICEL™ | 2024-05-08 ACTIVHEAL® RAPONICEL™ ULTRA 2.5X30.5CM |
| 15032749040667 - RAPONICEL™ | 2024-05-08 ACTIVHEAL® RAPONICEL™ ULTRA 2X46CM |