FDA UDI In Commercial Distribution 🇺🇸 United States

Acuitas

DI: 04260364751017 · Model: Curetis Qualified QuantStudio™ 5 Real-Time PCR System · Curetis GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Acuitas
Primary DI
04260364751017
Version / Model
Curetis Qualified QuantStudio™ 5 Real-Time PCR System
Catalog Number
62006
Company Name
Curetis GmbH
Labeler DUNS
312621863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-04-17
Public Version
2
Public Version Date
2023-05-26
Public Version Status
Update
Public Device Record Key
58ffde7a-143d-44a0-a760-9e5b788178fb

Device Description

QuantStudio Real-Time PCR Instrument qualified by Curetis for use with Acuitas AMR Gene Panel.

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OOI Real Time Nucleic Acid Amplification System

GMDN Terms

Code Name
48031 Thermal cycler nucleic acid amplification analyser IVD, laboratory

Identifiers

Type ID
Primary 04260364751017
Previous 20812125010062

Customer Contacts

Phone
301-869-9683

Premarket Submissions

Submission Number Supplement Number
K191288 000