FDA UDI In Commercial Distribution 🇺🇸 United States

NAMIC

DI: 10193489078091 · Model: H965914061 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NAMIC
Primary DI
10193489078091
Version / Model
H965914061
Catalog Number
H965914061
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-23
Public Version
1
Public Version Date
2022-03-03
Public Version Status
New
Public Device Record Key
d1c4e305-776c-44b7-b154-b03d2c23d961

Device Description

INFLATION DEVICE W/ LG BR Y ADAPT

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
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
OEQ Angiography/angioplasty kit

GMDN Terms

Code Name
17541 Catheter/overtube balloon inflator, single-use

Identifiers

Type ID
Package 20193489078098
Primary 10193489078091

Customer Contacts

Device Sizes

Type Value Unit Text
Pressure 3040 KiloPascal