FDA UDI In Commercial Distribution 🇺🇸 United States

CK-MB

DI: 05055273201420 · Model: CK1296 · RANDOX LABORATORIES LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
CK-MB
Primary DI
05055273201420
Version / Model
CK1296
Catalog Number
CK1296
Company Name
RANDOX LABORATORIES LIMITED
Labeler DUNS
227530649
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
b2815b02-0434-498b-ad93-530a6580a032

Device Description

The device is intended for the quantitative in vitro determination of CK-MB concentration in serum or plasma.

Device Characteristics

Single Use
Yes
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
CGS Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes

GMDN Terms

Code Name
52996 Creatine kinase myocardial isoenzyme (CKMB) IVD, reagent

Identifiers

Type ID
Primary 05055273201420

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K951223 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius