FDA UDI In Commercial Distribution 🇺🇸 United States

cobas®4800 System Liquid Cytology Preparation Kit

DI: 00875197003208 · Model: 05235839190 · Roche Molecular Systems, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
cobas®4800 System Liquid Cytology Preparation Kit
Primary DI
00875197003208
Version / Model
05235839190
Catalog Number
05235839190
Company Name
Roche Molecular Systems, Inc.
Labeler DUNS
071674100
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-11
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
510dafea-eaad-4d21-89f8-f587e58d5ce8

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
MAQ KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS

GMDN Terms

Code Name
49997 Human papillomavirus (HPV) high risk strain nucleic acid IVD, kit, nucleic acid technique (NAT)

Identifiers

Type ID
Primary 00875197003208