FDA UDI In Commercial Distribution 🇺🇸 United States

LUMIS™

DI: 03663136023656 · Model: MS1-MBASE1 · SPINEVISION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LUMIS™
Primary DI
03663136023656
Version / Model
MS1-MBASE1
Company Name
SPINEVISION
Labeler DUNS
390377518
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-02-03
Public Version
3
Public Version Date
2018-06-26
Public Version Status
Update
Public Device Record Key
219a915a-2a99-4079-8e66-0f76983c28f8

Device Description

LUMIS™ BASE 1 FOR INSTRUMENTS

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
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
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 03663136023656

Device Sizes

Type Value Unit Text
Device Size Text, specify 0