FDA UDI In Commercial Distribution 🇺🇸 United States

ERBE

DI: 08809083941765 · Model: 20190-168 · BIOPROTECH INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
ERBE
Primary DI
08809083941765
Version / Model
20190-168
Catalog Number
20190-168
Company Name
BIOPROTECH INC.
Labeler DUNS
688460539
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-08
Public Version
2
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
49166b09-98a8-4c5c-8fe0-bfcbc7854ed9

Device Description

rocker switch; holster; needle electrode; L 3m

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
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
44681 Electrosurgical handpiece, single-use

Identifiers

Type ID
Package 28809083941769
Package 18809083941762
Primary 08809083941765

Premarket Submissions

Submission Number Supplement Number
K092732 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-10 – 40 Degrees Celsius