FDA UDI In Commercial Distribution 🇺🇸 United States

ACURA Stabilization System

DI: B922F00500380 · Model: F005.0038 · INDIUS MEDICAL TECHNOLOGIES PRIVATE LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ACURA Stabilization System
Primary DI
B922F00500380
Version / Model
F005.0038
Catalog Number
F005.0038
Company Name
INDIUS MEDICAL TECHNOLOGIES PRIVATE LIMITED
Labeler DUNS
860396609
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-03-11
Public Version
1
Public Version Date
2026-03-19
Public Version Status
New
Public Device Record Key
43a441b6-cd15-4ad1-b9ab-99ebdd57d995

Device Description

Guidewire Extractor

Device Characteristics

Single Use
No
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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HWB Extractor

GMDN Terms

Code Name
63105 Orthopaedic instrument extractor

Identifiers

Type ID
Primary B922F00500380

Customer Contacts