FDA UDI In Commercial Distribution 🇺🇸 United States

Legato®

DI: 04250337103783 · Model: JMPH352504 · Joimax GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Legato®
Primary DI
04250337103783
Version / Model
JMPH352504
Company Name
Joimax GmbH
Labeler DUNS
344267187
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-08
Public Version
4
Public Version Date
2023-08-28
Public Version Status
Update
Public Device Record Key
3c1b3a33-262e-4521-ac63-5511bceb6d87

Device Description

Legato® Hand Piece, monopolar

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
No
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
44776 Electrosurgical system

Identifiers

Type ID
Primary 04250337103783

Customer Contacts

Phone
+49721255140

Premarket Submissions

Submission Number Supplement Number
K161378 000