FDA UDI In Commercial Distribution 🇺🇸 United States

Illico

DI: 00840967192840 · Model: 73770-18-4 · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Illico
Primary DI
00840967192840
Version / Model
73770-18-4
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-23
Public Version
3
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
a52a3936-5f0f-431f-ae58-d3699810ae53

Device Description

Blunt, Threaded Tip Nitinol Guidewire 17.75"

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
Yes
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
63819 Spinal guidewire

Identifiers

Type ID
Primary 00840967192840

Customer Contacts