FDA UDI Not in Commercial Distribution 🇺🇸 United States

STRADIS

DI: M7525050101 · Model: 505-010 · STRADIS MEDICAL, LLC
Product Codes
1
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
STRADIS
Primary DI
M7525050101
Version / Model
505-010
Company Name
STRADIS MEDICAL, LLC
Labeler DUNS
174262477
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-05-05
Public Version
5
Public Version Date
2022-03-25
Public Version Status
Update
Public Device Record Key
d546bf20-3f6c-4099-b3ae-979ff9e0ec6f
Distribution End Date
2022-03-24

Device Description

STERILE SEPARATES COTTON APPLICATOR 3"

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
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
KXG Applicator, Absorbent Tipped, Sterile

GMDN Terms

Code Name
33722 General-purpose absorbent tip applicator/swab, single-use

Identifiers

Type ID
Primary M7525050101

Customer Contacts

Phone
770-962-2425