FDA UDI In Commercial Distribution 🇺🇸 United States

Sklar

DI: 50649111448865 · Model: 96-2391M · SKLAR CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
Sklar
Primary DI
50649111448865
Version / Model
96-2391M
Company Name
SKLAR CORPORATION
Labeler DUNS
006966006
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2019-09-11
Public Version
1
Public Version Date
2019-09-19
Public Version Status
New
Public Device Record Key
7aa1a8c5-9a56-4d2a-aec0-d83525e4593f

Device Description

FOX DERMAL CUR SIZE 2 STRL CS/25

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HTF CURETTE

GMDN Terms

Code Name
63259 Dermal curette

Identifiers

Type ID
Primary 50649111448865
Unit of Use 00649111448860