FDA UDI In Commercial Distribution 🇺🇸 United States

POWERBLADE

DI: 00814334021972 · Model: 43933865 · Richard Wolf GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
POWERBLADE
Primary DI
00814334021972
Version / Model
43933865
Catalog Number
4393.3865
Company Name
Richard Wolf GmbH
Labeler DUNS
315304071
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2018-03-05
Public Version
4
Public Version Date
2019-04-23
Public Version Status
Update
Public Device Record Key
0f842086-3d1f-4907-aed5-13ceb2f04858

Device Description

CUT&COAG FORCEPS Ø 5MM WL 310MM BIPO for single use

Device Characteristics

Single Use
Yes
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
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
57944 Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

Identifiers

Type ID
Primary 00814334021972
Unit of Use 00814334021989

Customer Contacts

Phone
+497043350

Device Sizes

Type Value Unit Text
Outer Diameter 5 Millimeter
Length 310 Millimeter