FDA UDI In Commercial Distribution 🇺🇸 United States

AccuThrive®

DI: 00843382114336 · Model: Debridement Blade · AccuTec, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
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
AccuThrive®
Primary DI
00843382114336
Version / Model
Debridement Blade
Catalog Number
AVSC-3000-0000
Company Name
AccuTec, Inc.
Labeler DUNS
079966794
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-17
Public Version
1
Public Version Date
2024-12-25
Public Version Status
New
Public Device Record Key
5e5fe527-43b1-496b-81be-f1d287a57fc6

Device Description

ACCUTHRIVE DEBRIDEBLADE WOUND CARE BLADE SS STERILE USA 400BL/CA (50BL/CT, 8CT/CS)

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
MDM Instrument, Manual, Surgical, General Use

GMDN Terms

Code Name
63028 Skin biopsy blade

Identifiers

Type ID
Package 00843382114343
Primary 00843382114336
Package 00843382114350

Customer Contacts