FDA UDI In Commercial Distribution 🇺🇸 United States

n.a.

DI: 04048438001349 · Model: 031322-10 · Karl Storz GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
n.a.
Primary DI
04048438001349
Version / Model
031322-10
Company Name
Karl Storz GmbH & Co. KG
Labeler DUNS
315731430
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2019-02-23
Public Version
3
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
28d7248c-614e-4edb-8f97-f282aadfb4d6

Device Description

Insufflation Tubing Set, with gas filter

Device Characteristics

Single Use
Yes
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NKC Tubing/tubing with filter, insufflation, laparoscopic

GMDN Terms

Code Name
60738 Endoscopic insufflation tubing set, single-use

Identifiers

Type ID
Primary 04048438001349
Unit of Use 04048438001332