FDA UDI Not in Commercial Distribution 🇺🇸 United States

Neurologica

DI: 00618125183524 · Model: 30020F · TIDI PRODUCTS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Neurologica
Primary DI
00618125183524
Version / Model
30020F
Company Name
TIDI PRODUCTS, LLC
Labeler DUNS
063519193
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-07
Public Version
3
Public Version Date
2023-03-01
Public Version Status
Update
Public Device Record Key
0a96feda-f6b4-4b4f-bf73-2f0bc36ce86f
Distribution End Date
2023-02-28

Device Description

BOARD, HEAD & NECK ENT TABLE, 1 Each

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IWY Holder, Head, Radiographic

GMDN Terms

Code Name
13959 Instrument table

Identifiers

Type ID
Primary 00618125183524