FDA UDI Not in Commercial Distribution 🇺🇸 United States

i.Series®

DI: 00816394020834 · Model: PF396i · HELMER, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
i.Series®
Primary DI
00816394020834
Version / Model
PF396i
Company Name
HELMER, INC.
Labeler DUNS
086685682
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-01
Public Version
3
Public Version Date
2021-08-18
Public Version Status
Update
Public Device Record Key
8d7b8a29-2a7c-4ee6-a160-97600c66d174
Distribution End Date
2021-08-17

Device Description

Platelet Agitator

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KSQ Device, Blood Mixing And Blood Weighing

GMDN Terms

Code Name
45226 Platelet agitator

Identifiers

Type ID
Primary 00816394020834

Customer Contacts

Phone
317-773-9073