FDA UDI In Commercial Distribution 🇺🇸 United States

DAU NEGATIVE V3

DI: B800DAUNEGFV3UVHS0 · Model: DAU NEG F V3 UVHS · UTAK LABORATORIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
DAU NEGATIVE V3
Primary DI
B800DAUNEGFV3UVHS0
Version / Model
DAU NEG F V3 UVHS
Catalog Number
DAU NEG F V3 UVHS
Company Name
UTAK LABORATORIES, INC.
Labeler DUNS
092519016
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-09
Public Version
1
Public Version Date
2024-10-17
Public Version Status
New
Public Device Record Key
d5a8c488-1085-4b38-9286-8032b4501e5b

Device Description

DAU NEGATIVE V3

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
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
LAS Drug Specific Control Materials

GMDN Terms

Code Name
47869 Multiple-type clinical chemistry analyte profile IVD, control

Identifiers

Type ID
Package B800DAUNEGFV3UVHS5
Primary B800DAUNEGFV3UVHS0

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 5 Milliliter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– -10 Degrees Celsius