FDA UDI In Commercial Distribution 🇺🇸 United States

Sklar

DI: 10649111099786 · Model: 40-4225 · SKLAR CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sklar
Primary DI
10649111099786
Version / Model
40-4225
Company Name
SKLAR CORPORATION
Labeler DUNS
006966006
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-08-02
Public Version
1
Public Version Date
2019-08-12
Public Version Status
New
Public Device Record Key
c85385f3-6aba-4146-993e-f55167e8f058

Device Description

BIOPSY FCP 110° VERT CUT 4.75 IN

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
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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GEN FORCEPS, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
11775 Open-surgery biopsy forceps, reusable

Identifiers

Type ID
Primary 10649111099786