FDA UDI In Commercial Distribution 🇺🇸 United States

Swabeze

DI: 00817522013384 · Model: KMI-111 · KENTEC MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
50

Basic Information

Brand Name
Swabeze
Primary DI
00817522013384
Version / Model
KMI-111
Catalog Number
KMI-111
Company Name
KENTEC MEDICAL, INC.
Labeler DUNS
066175613
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2024-06-27
Public Version
1
Public Version Date
2024-07-05
Public Version Status
New
Public Device Record Key
c8a38d0a-97c8-498b-a78d-318e010aee79

Device Description

foam swab

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
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KXF Applicator, Absorbent Tipped, Non-Sterile

GMDN Terms

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

Identifiers

Type ID
Package 20817522013388
Primary 00817522013384
Package 30817522013385
Unit of Use 10817522013381