FDA UDI Not in Commercial Distribution 🇺🇸 United States

Quantum®

DI: 05020583920002 · Model: 92000 · TERUMO BCT, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Quantum®
Primary DI
05020583920002
Version / Model
92000
Company Name
TERUMO BCT, INC.
Labeler DUNS
801679200
Distribution Status
Not 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
06e893d2-81ca-4563-b2a5-f0e00d723330
Distribution End Date
2020-07-01

Device Description

Cell Expansion System

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
KJF SYSTEM, SUSPENSION, CELL CULTURE

GMDN Terms

Code Name
44904 Blood/tissue storage/culture container

Identifiers

Type ID
Primary 05020583920002

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
2 – 40 Degrees Celsius