FDA UDI In Commercial Distribution 🇺🇸 United States

AquaGuard

DI: 10618125192318 · Model: 50000-SMP · TIDI PRODUCTS, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
AquaGuard
Primary DI
10618125192318
Version / Model
50000-SMP
Catalog Number
50000-SMP
Company Name
TIDI PRODUCTS, LLC
Labeler DUNS
063519193
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-23
Public Version
1
Public Version Date
2025-10-01
Public Version Status
New
Public Device Record Key
2522ae8a-2b6c-46d0-8fe9-9f3e291078f5

Device Description

AG-SB, SAMPLE KIT

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
Yes
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
KIA Cover, Cast
KGX Tape And Bandage, Adhesive

GMDN Terms

Code Name
33536 Cast/bandage waterproof bathing cover, single-use

Identifiers

Type ID
Primary 10618125192318