FDA UDI In Commercial Distribution 🇺🇸 United States

Add Pack Hemo Control DM

DI: 04048534002189 · Model: 3040-7201-0099 · EKF-diagnostic GmbH
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Add Pack Hemo Control DM
Primary DI
04048534002189
Version / Model
3040-7201-0099
Catalog Number
3040-7201-0099
Company Name
EKF-diagnostic GmbH
Labeler DUNS
330046442
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-21
Public Version
1
Public Version Date
2022-12-29
Public Version Status
New
Public Device Record Key
64ab4269-f31f-47f4-85ed-d628f8f72f51

Device Description

For the quantitative determination of hemoglobin in whole blood.

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
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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GKR System, Hemoglobin, Automated
KHG Whole Blood Hemoglobin Determination

GMDN Terms

Code Name
32435 Haemoglobin analyser IVD, point-of-care

Identifiers

Type ID
Primary 04048534002189

Customer Contacts