FDA UDI Not in Commercial Distribution 🇺🇸 United States

CK-MB Test

DI: 00657498000748 · Model: 0980-103 · STANBIO LABORATORY, L.P.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CK-MB Test
Primary DI
00657498000748
Version / Model
0980-103
Catalog Number
0980-103
Company Name
STANBIO LABORATORY, L.P.
Labeler DUNS
045361136
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
4
Public Version Date
2023-07-06
Public Version Status
Update
Public Device Record Key
2398aad5-e821-4319-a8c4-6ed9a6359449
Distribution End Date
2022-08-30

Device Description

For the Quantitative Determination of Creatine Kinase-MB (CK-MB) in Serum for Manual and/or Automated Procedures.

Device Characteristics

Single Use
Yes
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
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
JHW U.V. Method, Cpk Isoenzymes

GMDN Terms

Code Name
52994 Creatine kinase myocardial isoenzyme (CKMB) IVD, kit, spectrophotometry

Identifiers

Type ID
Primary 00657498000748

Customer Contacts

Phone
18005315535

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius