FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04048551225776 · Model: 11009BI1 · Karl Storz GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04048551225776
Version / Model
11009BI1
Company Name
Karl Storz GmbH & Co. KG
Labeler DUNS
315731430
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
0df1163a-e218-4b0a-8441-a9e1f074e03f

Device Description

AF Broncho-Fiberscope 5.6x54

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["High-level Disinfectant", "Ethylene Oxide", "Liquid Chemical"]

Product Codes

Code Name
MRK System, Imaging, Fluorescence

GMDN Terms

Code Name
35461 Flexible fibreoptic bronchoscope

Identifiers

Type ID
Primary 04048551225776

Customer Contacts

Phone
424-218-8578

Premarket Submissions

Submission Number Supplement Number
P020008 000