FDA UDI Not in Commercial Distribution 🇺🇸 United States

Reprocessed 3.5mm VAPR Straight End Effect Electrode

DI: B3902253031 · Model: 227303 · SURETEK MEDICAL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Reprocessed 3.5mm VAPR Straight End Effect Electrode
Primary DI
B3902253031
Version / Model
227303
Company Name
SURETEK MEDICAL
Labeler DUNS
785616934
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-05
Public Version
2
Public Version Date
2021-06-17
Public Version Status
Update
Public Device Record Key
743aa5a7-ae7a-48d4-86c9-13c63ab575e8
Distribution End Date
2021-06-16

Device Description

Reprocessed 3.5mm VAPR Straight End Effect Electrode

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
No
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
NUJ Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

GMDN Terms

Code Name
61817 Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed

Identifiers

Type ID
Primary B3902253031

Premarket Submissions

Submission Number Supplement Number
K052692 000