FDA UDI In Commercial Distribution 🇺🇸 United States

Screw Caddy

DI: M739134000907 · Model: 13400-0907 · CAPTIVA SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Screw Caddy
Primary DI
M739134000907
Version / Model
13400-0907
Company Name
CAPTIVA SPINE, INC.
Labeler DUNS
836975784
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-29
Public Version
1
Public Version Date
2023-10-09
Public Version Status
New
Public Device Record Key
069caa43-1634-412e-b856-ad48aa9b3f09

Device Description

SmartLOX Screw Caddy

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
Yes
Has Lot/Batch Number
No
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
FSM Tray, Surgical, Instrument

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary M739134000907

Customer Contacts

Phone
561-277-9480