FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04048551186688 · Model: 649182E · Karl Storz GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
NA
Primary DI
04048551186688
Version / Model
649182E
Catalog Number
649182E
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
2025-03-28
Public Version
1
Public Version Date
2025-04-07
Public Version Status
New
Public Device Record Key
6f682b55-e7e4-4cc2-b92d-4cfefa541a3e

Device Description

Stylet for 649182

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
Yes
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, High-level Disinfectant, Moist Heat or Steam Sterilization, Hydrogen Peroxide, Liquid Chemical

Product Codes

Code Name
LRC INSTRUMENT, ENT MANUAL SURGICAL

GMDN Terms

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

Identifiers

Type ID
Primary 04048551186688

Customer Contacts

Phone
+14242188201