FDA UDI In Commercial Distribution 🇺🇸 United States

Synermed®

DI: 05060500090685 · Model: UV310-WK · INFRARED LABORATORY SYSTEMS LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Synermed®
Primary DI
05060500090685
Version / Model
UV310-WK
Catalog Number
UV310-WK
Company Name
INFRARED LABORATORY SYSTEMS LLC
Labeler DUNS
014210494
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-20
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
d3c35900-ff5c-40ea-84c5-864bb33cacb6

Device Description

Creatine Kinase Reagent 3 X 25 mL + 3 X 12.5 mL + 3 wedges

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
CGS Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes

GMDN Terms

Code Name
53006 Total creatine kinase (CK) IVD, reagent

Identifiers

Type ID
Primary 05060500090685

Customer Contacts

Phone
317 896-1565

Premarket Submissions

Submission Number Supplement Number
K930932 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 4 Degrees Celsius