FDA UDI In Commercial Distribution 🇺🇸 United States

DHI Specimen Collection System

DI: 30014613335450 · Model: 99-08019A · DIAGNOSTIC HYBRIDS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DHI Specimen Collection System
Primary DI
30014613335450
Version / Model
99-08019A
Catalog Number
99-08019A
Company Name
DIAGNOSTIC HYBRIDS, INC.
Labeler DUNS
117359612
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-28
Public Version
6
Public Version Date
2023-06-29
Public Version Status
Update
Public Device Record Key
565b50c2-905a-4174-b604-174bb3a23ba3

Device Description

3.0-ML UTM W/ FLEX NASOPHAR

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Sterilization Prior Use
No

Product Codes

Code Name
KXG APPLICATOR, ABSORBENT TIPPED, STERILE

GMDN Terms

Code Name
62773 General specimen collection kit IVD, clinical

Identifiers

Type ID
Primary 30014613335450

Customer Contacts