FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04048551308325 · Model: 11540KE · Karl Storz GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04048551308325
Version / Model
11540KE
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
4
Public Version Date
2019-03-11
Public Version Status
Update
Public Device Record Key
71cb3494-24d1-4822-bc19-023235848a88

Device Description

Operating Sheath, curved, size 3.3 mm

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
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
["Ethylene Oxide", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
HFA Amnioscope, Transabdominal (Fetoscope) (And Accessories)

GMDN Terms

Code Name
37086 Endoscope sheath, reusable

Identifiers

Type ID
Primary 04048551308325