FDA UDI In Commercial Distribution 🇺🇸 United States

Hospira

DI: 10887787006855 · Model: 795112 · HOSPIRA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
6

Basic Information

Brand Name
Hospira
Primary DI
10887787006855
Version / Model
795112
Catalog Number
0795112
Company Name
HOSPIRA, INC.
Labeler DUNS
141588017
Distribution Status
In Commercial Distribution
Device Count in Pkg
6
Record Status
Published
Publish Date
2016-09-01
Public Version
4
Public Version Date
2021-04-07
Public Version Status
Update
Public Device Record Key
ded8e873-b23a-42af-84fe-569a6b4852e0

Device Description

250 mL EMPTY CONTAINER

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
58977 Basic intravenous administration set, noninvasive

Identifiers

Type ID
Package 20887787006852
Primary 10887787006855
Secondary M3357951122
Unit of Use 00887787006858

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 250 Milliliter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Room Temperature. Avoid Excessive Heat. Protect from Freezing