FDA UDI In Commercial Distribution 🇺🇸 United States

SPOTCHECK

DI: 00725609000472 · Model: 82-0200-01K · ASTORIA-PACIFIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SPOTCHECK
Primary DI
00725609000472
Version / Model
82-0200-01K
Catalog Number
82-0200-01K
Company Name
ASTORIA-PACIFIC, INC.
Labeler DUNS
623238615
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-17
Public Version
1
Public Version Date
2020-12-25
Public Version Status
New
Public Device Record Key
a578b315-032f-444c-8c81-ae16724c9045

Device Description

MS/MS Positive 1 Control Card

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
Yes
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
OHQ Multi-Analyte Controls Unassayed

GMDN Terms

Code Name
58192 Multiple amino acid/carnitine metabolite IVD, control

Identifiers

Type ID
Primary 00725609000472