FDA UDI In Commercial Distribution 🇺🇸 United States

MODUS

DI: 07630037850397 · Model: M-6720 · Medartis AG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MODUS
Primary DI
07630037850397
Version / Model
M-6720
Catalog Number
M-6720
Company Name
Medartis AG
Labeler DUNS
480054895
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-02-10
Public Version
2
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
2d594ff0-8759-4812-bb61-5ae115617903

Device Description

Holding Rack f.Case,240x240mm,Height7-12

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

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KCT Sterilization wrap containers, trays, cassettes & other accessories

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Previous 07630008491451
Primary 07630037850397

Premarket Submissions

Submission Number Supplement Number
K202589 000