FDA UDI Not in Commercial Distribution 🇺🇸 United States

Eurotrol

DI: 08718734960928 · Model: 183.000.005 · Eurotrol B.V.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Eurotrol
Primary DI
08718734960928
Version / Model
183.000.005
Company Name
Eurotrol B.V.
Labeler DUNS
412925992
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-12
Public Version
4
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
887fe105-fcc2-49d2-88c0-690ee89f2a82
Distribution End Date
2021-07-31

Device Description

Product is packaged in Eurotrol boxes, containing 5 ampules, one ampule of each level. It is a convenience kit for the purposes of UDI compliance because it contains 5 different levels that are packaged together for the convenience of the user and intended to remain packaged together and not replaced, substituted, repackaged, sterilized or otherwise processed or modified before being used by an end user. Therefore, the label of each individual vial within the container is not required to bear a UDI,provided that a UDI is available on the label affixed to the immediate container of the kit .

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JJY Multi-Analyte Controls, All Kinds (Assayed)

GMDN Terms

Code Name
52860 Multiple blood gas/haemoximetry/electrolyte analyte IVD, control

Identifiers

Type ID
Primary 08718734960928

Premarket Submissions

Submission Number Supplement Number
K121468 000