FDA UDI In Commercial Distribution 🇺🇸 United States

Signature Series

DI: 08714729875604 · Model: M0068805510 · PROSURG INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Signature Series
Primary DI
08714729875604
Version / Model
M0068805510
Company Name
PROSURG INC
Labeler DUNS
188684609
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-30
Public Version
4
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
8b6fdab6-5f12-4d67-8a56-756807474002

Device Description

Electrosurgical Devices, Incision Blade

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
FAS Electrode, Electrosurgical, Active, Urological

GMDN Terms

Code Name
44776 Electrosurgical system

Identifiers

Type ID
Package 08714729520658
Primary 08714729875604

Customer Contacts

Phone
408 945 4044

Premarket Submissions

Submission Number Supplement Number
K962593 000

Device Sizes

Type Value Unit Text
Catheter Gauge 24 French