FDA UDI In Commercial Distribution 🇺🇸 United States

Lumipulse G Mesothelin Calibrator

DI: 04987270233436 · Model: 233436 · FUJIREBIO INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Lumipulse G Mesothelin Calibrator
Primary DI
04987270233436
Version / Model
233436
Company Name
FUJIREBIO INC.
Labeler DUNS
710873907
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-02-01
Public Version
6
Public Version Date
2023-02-09
Public Version Status
Update
Public Device Record Key
2caef70e-007d-48c7-8888-62a12375da76

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
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
No
Sterilization Prior Use
No

Product Codes

Code Name
OAW Cancer Monitoring Test System, Soluble Mesothelin-Related Peptides, Epithelioid/Biphasic Mesothelioma

GMDN Terms

Code Name
63470 Soluble mesothelin-related peptide (SMRP) IVD, calibrator

Identifiers

Type ID
Primary 04987270233436

Customer Contacts

Phone
610-240-3800

Device Sizes

Type Value Unit Text
Device Size Text, specify Size Type = Units per kit; Units = 3; Unit of Measure = 4.5mLs

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Right side up with care; no vibration
Type
Storage Environment Temperature
Temperature Range
2 – 10 Degrees Celsius
Type
Handling Environment Temperature
Temperature Range
2 – 10 Degrees Celsius