FDA UDI In Commercial Distribution 🇺🇸 United States

Spectra Optia®

DI: 05020583610002 · Model: 61000 · TERUMO BCT, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Spectra Optia®
Primary DI
05020583610002
Version / Model
61000
Company Name
TERUMO BCT, INC.
Labeler DUNS
801679200
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-15
Public Version
7
Public Version Date
2023-07-24
Public Version Status
Update
Public Device Record Key
6811bcea-6766-4bb8-9750-37c83ef811e9

Device Description

Spectra Optia® Apheresis System

Device Characteristics

Single Use
No
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
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
GKT Separator, automated, blood cell, diagnostic

GMDN Terms

Code Name
16405 Apheresis system

Identifiers

Type ID
Primary 05020583610002

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep out of sunlight.
Type
Special Storage Condition, Specify
Special Conditions
Protect from rain
Type
Storage Environment Temperature
Temperature Range
0 – 60 Degrees Celsius