FDA UDI In Commercial Distribution 🇺🇸 United States

Hometa

DI: 00850024592049 · Model: 60012 · Hometa, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Hometa
Primary DI
00850024592049
Version / Model
60012
Company Name
Hometa, Inc.
Labeler DUNS
117613680
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-11-14
Public Version
1
Public Version Date
2020-11-23
Public Version Status
New
Public Device Record Key
f5b34136-70d8-435d-9479-cbab7e1420ab

Device Description

Empty EVA Bags 2000mL

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
KPE Container, I.V.

GMDN Terms

Code Name
35127 Intravenous administration bag/bottle

Identifiers

Type ID
Package 10850024592046
Primary 00850024592049
Previous 00850002046366