FDA UDI Not in Commercial Distribution 🇺🇸 United States

Mermaid Medical

DI: 28481750004016 · Model: A20100090 · TIDI PRODUCTS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Mermaid Medical
Primary DI
28481750004016
Version / Model
A20100090
Catalog Number
A20100090
Company Name
TIDI PRODUCTS, LLC
Labeler DUNS
063519193
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-12
Public Version
2
Public Version Date
2023-03-06
Public Version Status
Update
Public Device Record Key
3bc28cf1-0977-4af5-8cc0-a96dbd0d9d4f
Distribution End Date
2023-03-05

Device Description

Mermaid Medical Specialty Securement Device - Drainage Tube White Loop/Liner/Hook/Foam/Bandage Sterile Extra Small

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
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 18481750004040
Primary 28481750004016
Package 00848175000407