FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 04055207061145 · Model: 8393793 · Richard Wolf GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04055207061145
Version / Model
8393793
Catalog Number
8393.793
Company Name
Richard Wolf GmbH
Labeler DUNS
315304071
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-21
Public Version
5
Public Version Date
2023-05-26
Public Version Status
Update
Public Device Record Key
19fe3606-b1d2-40b9-9085-d8ecef31604a
Distribution End Date
2018-11-30

Device Description

COAGULATION FORCEPS BIPO Ø 5MM BNDL 4 part, SL 300mm

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
No
PM Exempt
No
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
32684 Endoscopic electrosurgical handpiece/electrode, bipolar, reusable

Identifiers

Type ID
Primary 04055207061145

Customer Contacts

Phone
+497043350

Device Sizes

Type Value Unit Text
Outer Diameter 5 Millimeter