FDA UDI In Commercial Distribution 🇺🇸 United States

Rhinostics, Inc.

DI: 00850042963111 · Model: GW-UF100001 · Rhinostics Inc
Product Codes
1
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Rhinostics, Inc.
Primary DI
00850042963111
Version / Model
GW-UF100001
Company Name
Rhinostics Inc
Labeler DUNS
100216104
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-24
Public Version
1
Public Version Date
2023-04-03
Public Version Status
New
Public Device Record Key
9388a377-5194-4a26-b7a6-4dd18893fe45

Device Description

GrooveSwab Sterile Collection Swab with Non-Flocked Tip

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
No
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
66225 General specimen collection kit IVD, home-use
57940 Oral/upper respiratory tract specimen collection swab

Identifiers

Type ID
Primary 00850042963111
Package 00850042963173