FDA UDI In Commercial Distribution 🇺🇸 United States

Removal Kit

DI: 03662663079938 · Model: 904R0004 · Highridge Medical, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Removal Kit
Primary DI
03662663079938
Version / Model
904R0004
Catalog Number
904R0004
Company Name
Highridge Medical, LLC
Labeler DUNS
119260394
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-16
Public Version
1
Public Version Date
2025-10-24
Public Version Status
New
Public Device Record Key
7e79ef53-3d50-457d-8d1b-9c18f6fdad62

Device Description

SILHOUETTE POLY SCREW REM TOOL

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
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
HXX SCREWDRIVER

GMDN Terms

Code Name
33968 Surgical screwdriver, reusable

Identifiers

Type ID
Primary 03662663079938

Customer Contacts