FDA UDI In Commercial Distribution 🇺🇸 United States

Arcus

DI: 00190376215877 · Model: 16122-01 · ALPHATEC SPINE, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Arcus
Primary DI
00190376215877
Version / Model
16122-01
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-01
Public Version
1
Public Version Date
2019-12-09
Public Version Status
New
Public Device Record Key
f35ff15e-56e8-4bd7-addd-7d38ebaa9ec2

Device Description

Arcus Stimulating Targeting Needle, Diamond Tip

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
No
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
PDQ Neurosurgical nerve locator
ETN STIMULATOR, NERVE

GMDN Terms

Code Name
46566 Neurophysiologic monitoring system

Identifiers

Type ID
Primary 00190376215877

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K191723 000