FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04055207022085 · Model: 8920311 · Richard Wolf GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04055207022085
Version / Model
8920311
Catalog Number
8920.311
Company Name
Richard Wolf GmbH
Labeler DUNS
315304071
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-28
Public Version
4
Public Version Date
2018-09-21
Public Version Status
Update
Public Device Record Key
573b668b-a1e6-41f8-b8d8-4bd91e840e79

Device Description

AUTOMATIC VALVE ID 5.7MM 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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Moist Heat or Steam Sterilization", "Hydrogen Peroxide", "Ethylene Oxide"]

Product Codes

Code Name
GCJ Laparoscope, general & plastic surgery

GMDN Terms

Code Name
37090 Endoscope assembly adaptor

Identifiers

Type ID
Primary 04055207022085

Customer Contacts

Phone
+497043350

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 5.7 Millimeter