FDA UDI In Commercial Distribution 🇺🇸 United States

Medtronic

DI: B504CB2331410 · Model: 23-314-1 · Provision
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Medtronic
Primary DI
B504CB2331410
Version / Model
23-314-1
Company Name
Provision
Labeler DUNS
016889401
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-23
Public Version
3
Public Version Date
2021-03-01
Public Version Status
Update
Public Device Record Key
ae600109-57c9-4eff-a828-54c74b4a7b50

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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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 B504CB2331410

Customer Contacts

Phone
541-480-7953

Premarket Submissions

Submission Number Supplement Number
K172647 000