FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 04055207015544 · Model: 8391204 · Richard Wolf GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04055207015544
Version / Model
8391204
Catalog Number
8391.204
Company Name
Richard Wolf GmbH
Labeler DUNS
315304071
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-28
Public Version
5
Public Version Date
2023-05-26
Public Version Status
Update
Public Device Record Key
4840bda7-9ab9-4dd7-9bd9-877fea46be28
Distribution End Date
2018-11-30

Device Description

GRASP. FORCEPS INSERT SHEATH Ø 3.5MM atraumatic, fine cross toothing, WL 330mm, double action, insulated sheath with flushing port, 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", "Ethylene Oxide"]

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
33596 Endoscopic electrosurgical handpiece/electrode, monopolar, reusable

Identifiers

Type ID
Primary 04055207015544

Customer Contacts

Phone
+497043350

Device Sizes

Type Value Unit Text
Outer Diameter 3.5 Millimeter