FDA UDI In Commercial Distribution 🇺🇸 United States

Inflow cannula

DI: 04059082033242 · Model: 191 501 600 · SOPRO-COMEG GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Inflow cannula
Primary DI
04059082033242
Version / Model
191 501 600
Company Name
SOPRO-COMEG GmbH
Labeler DUNS
507185952
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-20
Public Version
1
Public Version Date
2018-04-20
Public Version Status
New
Public Device Record Key
197c99c8-81e5-45aa-93a7-97e25af0a4d7

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
HRX Arthroscope

GMDN Terms

Code Name
45254 Suction cannula, reusable

Identifiers

Type ID
Primary 04059082033242