FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10080196759705 · Model: DYNJAAPI500T · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10080196759705
Version / Model
DYNJAAPI500T
Catalog Number
DYNJAAPI500T
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-03
Public Version
2
Public Version Date
2024-02-23
Public Version Status
Update
Public Device Record Key
b0a0ffbe-b1e1-4a20-9947-00df60405745

Device Description

500ML,PRESSURE INFUSER W/THUMBWHEEL

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KZD INFUSOR, PRESSURE, FOR I.V. BAGS

GMDN Terms

Code Name
65172 Intravenous pressure infusor, manual, single-use

Identifiers

Type ID
Primary 10080196759705
Package 40080196759706

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry. Keep away from sunlight