FDA UDI In Commercial Distribution 🇺🇸 United States

ERBE

DI: 04050147018402 · Model: 20189-311 · Erbe Elektromedizin GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ERBE
Primary DI
04050147018402
Version / Model
20189-311
Catalog Number
20189-311
Company Name
Erbe Elektromedizin GmbH
Labeler DUNS
316116623
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-10
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
b975ea68-1c00-47b2-a564-4bc6d1cc3b3d

Device Description

VIO® 2-pedal footsw.; ReMode® AP & IP X8 Equipment; US

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
No

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
36336 Foot-switch, electrical

Identifiers

Type ID
Primary 04050147018402

Customer Contacts

Phone
+4970717550

Premarket Submissions

Submission Number Supplement Number
K083452 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry
Type
Special Storage Condition, Specify
Special Conditions
Keep away from heat and direct sunlight