FDA UDI In Commercial Distribution 🇺🇸 United States

ERAGON BIPOLAR

DI: 04055207033876 · Model: 839300102 · Richard Wolf GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ERAGON BIPOLAR
Primary DI
04055207033876
Version / Model
839300102
Catalog Number
839300102
Company Name
Richard Wolf GmbH
Labeler DUNS
315304071
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-27
Public Version
5
Public Version Date
2021-04-28
Public Version Status
Update
Public Device Record Key
7845f9d0-9425-4728-9ac0-a1f70eb02b08

Device Description

HANDLE PISTOL SHAPED BIPO without locking mechanism, with bipolar HF-connection, for use with all bipolar ERAGON outer sheath tubes, reusable

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HET LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES)

GMDN Terms

Code Name
32684 Endoscopic electrosurgical handpiece/electrode, bipolar, reusable

Identifiers

Type ID
Primary 04055207033876

Customer Contacts

Phone
+497043350