FDA UDI In Commercial Distribution 🇺🇸 United States

Actibride™

DI: 15032749039166 · Model: Debridement Pad · ADVANCED MEDICAL SOLUTIONS LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Actibride™
Primary DI
15032749039166
Version / Model
Debridement Pad
Catalog Number
9039169
Company Name
ADVANCED MEDICAL SOLUTIONS LIMITED
Labeler DUNS
770434090
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-30
Public Version
2
Public Version Date
2025-04-18
Public Version Status
Update
Public Device Record Key
5b27fcad-d527-4051-8f3a-afb7cb2229ea

Device Description

ActivHeal® Actibride™ Debridement Pad 11cmx18cm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NAB Gauze / Sponge,Nonresorbable For External Use

GMDN Terms

Code Name
48134 Woven gauze pad, non-antimicrobial

Identifiers

Type ID
Primary 15032749039166