FDA UDI In Commercial Distribution 🇺🇸 United States

Spineart Surgical Illuminator

DI: 00812432021429 · Model: 008612 · LUMITEX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Spineart Surgical Illuminator
Primary DI
00812432021429
Version / Model
008612
Catalog Number
MIS-IN 44 00-S
Company Name
LUMITEX, INC.
Labeler DUNS
108631797
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-30
Public Version
1
Public Version Date
2020-10-08
Public Version Status
New
Public Device Record Key
47455f97-095c-424a-94f6-4ff59383f226

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FDG Retractor, Fiberoptic

GMDN Terms

Code Name
48036 Surgical instrument fibreoptic light

Identifiers

Type ID
Primary 00812432021429