FDA UDI In Commercial Distribution 🇺🇸 United States

n.a.

DI: 04048551067970 · Model: 204001 · Karl Storz GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
n.a.
Primary DI
04048551067970
Version / Model
204001
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
2016-09-23
Public Version
5
Public Version Date
2020-04-20
Public Version Status
Update
Public Device Record Key
a46c6804-e710-451e-8a59-6b69f544557f

Device Description

Suction Handle, 10 cm

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
["Moist Heat or Steam Sterilization", "Hydrogen Peroxide", "Ethylene Oxide", "Peracetic Acid"]

Product Codes

Code Name
EOX ESOPHAGOSCOPE (FLEXIBLE OR RIGID)

GMDN Terms

Code Name
38749 Surgical/emergency suction cannula, non-illuminating, reusable

Identifiers

Type ID
Primary 04048551067970

Premarket Submissions

Submission Number Supplement Number
K945237 000