FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04048551069530 · Model: 204809E · 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
04048551069530
Version / Model
204809E
Catalog Number
204809E
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
e4faa1e8-4100-4133-8921-b957ffe86aaf

Device Description

Mandrin, for 204809

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
Moist Heat or Steam Sterilization

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 04048551069530

Customer Contacts

Phone
+14242188201