FDA UDI Not in Commercial Distribution 🇺🇸 United States

Kew Medical

DI: 10816415020246 · Model: QEG4170 · DOUGLAS MEDICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
Kew Medical
Primary DI
10816415020246
Version / Model
QEG4170
Company Name
DOUGLAS MEDICAL PRODUCTS, INC.
Labeler DUNS
121040922
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2017-09-15
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
da12284d-d82a-40d6-bca6-a0326b97bb2f
Distribution End Date
2017-09-15

Device Description

9" IV Extension Set, 15 Micron Screen, Male Luer Lock (0.23m) Length- Box

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
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
FPA Set, Administration, Intravascular

GMDN Terms

Code Name
12170 Intravenous administration tubing extension set

Identifiers

Type ID
Primary 10816415020246
Unit of Use 00816415020249

Premarket Submissions

Submission Number Supplement Number
K925430 000