FDA UDI In Commercial Distribution 🇺🇸 United States

Dade® Data-Fi® Abnormal Fibrinogen Control

DI: 00842768003936 · Model: 10445719 · Siemens Healthcare Diagnostics Products GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Dade® Data-Fi® Abnormal Fibrinogen Control
Primary DI
00842768003936
Version / Model
10445719
Catalog Number
B4233-22
Company Name
Siemens Healthcare Diagnostics Products GmbH
Labeler DUNS
388240673
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-09-24
Public Version
6
Public Version Date
2024-02-21
Public Version Status
Update
Public Device Record Key
ead29129-8277-4587-a17d-991b77ce14f1

Device Description

Assessment of accuracy and precision of Dade® Fibrinogen Determination Reagents in the low range

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
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
KQJ SYSTEM, FIBRINOGEN DETERMINATION

GMDN Terms

Code Name
32393 Fibrinogen assay (factor I) IVD, control

Identifiers

Type ID
Primary 00842768003936
Unit of Use 00842768019524

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K811069 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius