FDA UDI In Commercial Distribution 🇺🇸 United States

MEDEASY

DI: 08054301665804 · Model: ML18250-K0 · MEDAX SRL UNIPERSONALE
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MEDEASY
Primary DI
08054301665804
Version / Model
ML18250-K0
Company Name
MEDAX SRL UNIPERSONALE
Labeler DUNS
440211428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-08-09
Public Version
2
Public Version Date
2023-02-06
Public Version Status
Update
Public Device Record Key
8171fd37-42fb-4150-8ea4-b11a79e41f56

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
Yes
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KNW Instrument, Biopsy

GMDN Terms

Code Name
16835 Soft-tissue biopsy procedure kit, non-medicated

Identifiers

Type ID
Package 18054301665801
Primary 08054301665804

Premarket Submissions

Submission Number Supplement Number
K181803 000