FDA UDI In Commercial Distribution 🇺🇸 United States

Sklar®

DI: 10649111003875 · Model: 91-6101 · SKLAR CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sklar®
Primary DI
10649111003875
Version / Model
91-6101
Company Name
SKLAR CORPORATION
Labeler DUNS
006966006
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-04
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
d27bf756-c6c3-4f6c-b36d-7978a2d11984

Device Description

BIPOLAR COAPT FCP .5MM 4"

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
47848 Open-surgery electrosurgical handpiece/electrode, bipolar, reusable

Identifiers

Type ID
Primary 10649111003875

Premarket Submissions

Submission Number Supplement Number
K964176 000