FDA UDI In Commercial Distribution 🇺🇸 United States

Reprocessed TAC-C II Probe

DI: B3907209628ST1 · Model: 7209628ST · SURETEK MEDICAL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Reprocessed TAC-C II Probe
Primary DI
B3907209628ST1
Version / Model
7209628ST
Company Name
SURETEK MEDICAL
Labeler DUNS
785616934
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-14
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
2b3f0c3c-78c8-4d25-bc0d-ae5749bc89de

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 B3907209628ST1

Premarket Submissions

Submission Number Supplement Number
K052692 000