FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10197344020508 · Model: DYNJAAPI500B · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10197344020508
Version / Model
DYNJAAPI500B
Catalog Number
DYNJAAPI500B
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-12-21
Public Version
1
Public Version Date
2023-12-29
Public Version Status
New
Public Device Record Key
70c44fec-b329-406e-8d2e-67a3caa3587b

Device Description

500ML,PRESSURE INFUSER W/STOPCOCK

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
13100 Intravenous pressure infusor, manual, reusable

Identifiers

Type ID
Package 20197344020505
Primary 10197344020508

Customer Contacts

Storage Conditions

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