FDA UDI Not in Commercial Distribution 🇺🇸 United States

MODULINE

DI: 04055207026502 · Model: 83930008 · Richard Wolf GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MODULINE
Primary DI
04055207026502
Version / Model
83930008
Catalog Number
8393.0008
Company Name
Richard Wolf GmbH
Labeler DUNS
315304071
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
6
Public Version Date
2023-05-26
Public Version Status
Update
Public Device Record Key
5fbcb37b-2fe8-49fa-9cdc-fb6a9b518e74
Distribution End Date
2018-11-30

Device Description

HANDLE PISTOL SHAPED with locking mechanism, non-rotatable, without HF-connection, for use with Moduline and RIWO-GRIP 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
["Ethylene Oxide", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
35732 Rigid endoscopic biopsy forceps, reusable

Identifiers

Type ID
Primary 04055207026502

Customer Contacts

Phone
+497043350