FDA UDI Not in Commercial Distribution 🇺🇸 United States

TIDI

DI: 01618125154066 · Model: 30852 · TIDI PRODUCTS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
TIDI
Primary DI
01618125154066
Version / Model
30852
Company Name
TIDI PRODUCTS, LLC
Labeler DUNS
063519193
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-13
Public Version
3
Public Version Date
2023-03-01
Public Version Status
Update
Public Device Record Key
f1c6e485-36db-4398-94f8-2f259d34fc97
Distribution End Date
2023-02-28

Device Description

Practitioner Positioning Black

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KKJ Sudan Iii

GMDN Terms

Code Name
13959 Instrument table

Identifiers

Type ID
Package 00618125154067
Primary 01618125154066