FDA UDI In Commercial Distribution 🇺🇸 United States

ELMED

DI: 00842180107953 · Model: 5709M/B · ELMED INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ELMED
Primary DI
00842180107953
Version / Model
5709M/B
Catalog Number
5709M/B
Company Name
ELMED INCORPORATED
Labeler DUNS
049290364
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-25
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
900cbe47-7a87-4bfe-a2f9-90cc20644c9f

Device Description

DOUBLE PEDAL, UL-APPROVED FOOTSWITCH - MONOPOLAR/BIPOLAR

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
36336 Foot-switch, electrical

Identifiers

Type ID
Primary 00842180107953

Customer Contacts

Phone
224-353-6446