FDA UDI In Commercial Distribution 🇺🇸 United States

Plan 1 Health

DI: 00618125135318 · Model: 03.06.70.10 · TIDI PRODUCTS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Plan 1 Health
Primary DI
00618125135318
Version / Model
03.06.70.10
Catalog Number
03.06.70.10
Company Name
TIDI PRODUCTS, LLC
Labeler DUNS
063519193
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-18
Public Version
1
Public Version Date
2022-10-26
Public Version Status
New
Public Device Record Key
a4f441da-ecb1-452b-8e0e-3db959eee5f8

Device Description

Medium Sized Securement Device, Intended for further processing

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KMK Device, Intravascular Catheter Securement

GMDN Terms

Code Name
56631 Wearable percutaneous catheter/tube holder

Identifiers

Type ID
Package 10618125135315
Primary 00618125135318