FDA UDI Not in Commercial Distribution 🇺🇸 United States

HiMax

DI: 00810112597752 · Model: 20mm CrossBar Guide - Body · CROSSROADS EXTREMITY SYSTEMS
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
HiMax
Primary DI
00810112597752
Version / Model
20mm CrossBar Guide - Body
Catalog Number
260297PKG
Company Name
CROSSROADS EXTREMITY SYSTEMS
Labeler DUNS
058864308
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-07
Public Version
2
Public Version Date
2024-08-23
Public Version Status
Update
Public Device Record Key
f13a9553-77b0-46da-970d-2ff6e3956f99
Distribution End Date
2024-08-22

Device Description

20mm CrossBar Guide - Body

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
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
FZX Guide, Surgical, Instrument

GMDN Terms

Code Name
35095 Surgical drill guide, reusable

Identifiers

Type ID
Primary 00810112597752