FDA UDI In Commercial Distribution 🇺🇸 United States

Sklar Instruments

DI: 10649111501326 · Model: 31-4074 · SKLAR CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sklar Instruments
Primary DI
10649111501326
Version / Model
31-4074
Company Name
SKLAR CORPORATION
Labeler DUNS
006966006
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-03-12
Public Version
1
Public Version Date
2026-03-20
Public Version Status
New
Public Device Record Key
e69010d9-cdfe-4c8f-9d5a-f73fb91d9f23

Device Description

WAVE GRASP DOUBLE ACTION 5MM, 450MM

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
MR Unsafe
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GCJ Laparoscope, general & plastic surgery

GMDN Terms

Code Name
62667 Laparoscopic tissue manipulation forceps/working-channel

Identifiers

Type ID
Primary 10649111501326