FDA UDI In Commercial Distribution 🇺🇸 United States

Dale Catheter Securement Device

DI: 00817612020124 · Model: 850 · DALE MEDICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Dale Catheter Securement Device
Primary DI
00817612020124
Version / Model
850
Catalog Number
850
Company Name
DALE MEDICAL PRODUCTS, INC.
Labeler DUNS
001061233
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-10
Public Version
3
Public Version Date
2019-07-22
Public Version Status
Update
Public Device Record Key
80ea423d-ea79-44f9-817e-2a025f1e900d

Device Description

Dale IV, Arterial and Mid-line Catheter Securement Device

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
Yes
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
KMK Device, Intravascular Catheter Securement

GMDN Terms

Code Name
56631 Wearable percutaneous catheter/tube holder

Identifiers

Type ID
Package 00817612020131
Primary 00817612020124

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Cool dry place