FDA UDI In Commercial Distribution 🇺🇸 United States

INFLOW CANNULA SHEATH

DI: 00192896094871 · Model: SC95-05599 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
INFLOW CANNULA SHEATH
Primary DI
00192896094871
Version / Model
SC95-05599
Catalog Number
SC95-05599
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-07
Public Version
4
Public Version Date
2023-06-26
Public Version Status
Update
Public Device Record Key
ac7ae695-840d-4a5d-b924-eed7e29c3a85

Device Description

INFLOW CANNULA SHEATH

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
Yes
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
["Dry Heat Sterilization", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
62458 Arthroscopic access cannula, reusable

Identifiers

Type ID
Primary 00192896094871

Customer Contacts