FDA UDI In Commercial Distribution 🇺🇸 United States

Reprocessed 4mm EndoScrub Sheath, 0 deg

DI: B39019120501 · Model: 19-12050 · SURETEK MEDICAL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Reprocessed 4mm EndoScrub Sheath, 0 deg
Primary DI
B39019120501
Version / Model
19-12050
Company Name
SURETEK MEDICAL
Labeler DUNS
785616934
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-19
Public Version
2
Public Version Date
2026-01-12
Public Version Status
Update
Public Device Record Key
b225cac7-a0ad-4987-9ce2-2f5cb9525cbb

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
KAM Cannula, Sinus

GMDN Terms

Code Name
48141 Paranasal sinus irrigation catheter

Identifiers

Type ID
Primary B39019120501