FDA UDI In Commercial Distribution 🇺🇸 United States

TIDI

DI: 00618125187072 · Model: 9012-D · TIDI PRODUCTS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TIDI
Primary DI
00618125187072
Version / Model
9012-D
Company Name
TIDI PRODUCTS, LLC
Labeler DUNS
063519193
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-29
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
851e21ba-987d-4ee5-9786-43193df74b1c

Device Description

TIDI Ct Accessories Infant 1 per 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
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KXJ Table, Radiologic

GMDN Terms

Code Name
41058 Multifunction body cushion

Identifiers

Type ID
Primary 00618125187072