FDA UDI In Commercial Distribution 🇺🇸 United States

Sklar®

DI: 40649111386597 · Model: 21-915 · SKLAR CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
12

Basic Information

Brand Name
Sklar®
Primary DI
40649111386597
Version / Model
21-915
Company Name
SKLAR CORPORATION
Labeler DUNS
006966006
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2018-08-08
Public Version
3
Public Version Date
2019-08-21
Public Version Status
Update
Public Device Record Key
9dab9b20-1940-4161-8a51-0ea754bc5e75

Device Description

JEWELER FORCEP #1 4.5" BX12

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
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
62479 Surgical soft-tissue manipulation forceps, tweezers-like, single-use

Identifiers

Type ID
Primary 40649111386597
Unit of Use 00649111386599