FDA UDI In Commercial Distribution 🇺🇸 United States

Screw Aligner

DI: M73922017001 · Model: 2201-7001 · CAPTIVA SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Screw Aligner
Primary DI
M73922017001
Version / Model
2201-7001
Company Name
CAPTIVA SPINE, INC.
Labeler DUNS
836975784
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-19
Public Version
1
Public Version Date
2022-07-27
Public Version Status
New
Public Device Record Key
79683081-96e4-4b7f-a823-0a021fba45f5

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
47870 Orthopaedic fixation implant alignment tool

Identifiers

Type ID
Primary M73922017001

Customer Contacts

Phone
561-277-9480