FDA UDI In Commercial Distribution 🇺🇸 United States

Repatha Pushtronex System

DI: 00355513770019 · Model: 9002870 · AMGEN INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Repatha Pushtronex System
Primary DI
00355513770019
Version / Model
9002870
Company Name
AMGEN INC.
Labeler DUNS
039976196
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-09-24
Public Version
1
Public Version Date
2019-10-02
Public Version Status
New
Public Device Record Key
eb34cc76-f0e7-4ab9-b0ec-73c8aa905977

Device Description

On-Body Infusor and Prefilled Cartridge

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
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
FRN Pump, Infusion

GMDN Terms

Code Name
44127 Autoinjector needle

Identifiers

Type ID
Package 10355513770016
Primary 00355513770019

Device Sizes

Type Value Unit Text
Total Volume 3.5 Milliliter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep out of the sight and reach of children
Type
Special Storage Condition, Specify
Special Conditions
Keep Dry
Type
Handling Environment Humidity
Temperature Range
15 – 85 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Store in Carton to Protect from Light
Type
Special Storage Condition, Specify
Special Conditions
Do Not Freeze or Shake