FDA UDI In Commercial Distribution 🇺🇸 United States

Sklar®

DI: 50649111400801 · Model: 96-2551M · SKLAR CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
Sklar®
Primary DI
50649111400801
Version / Model
96-2551M
Company Name
SKLAR CORPORATION
Labeler DUNS
006966006
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2018-08-10
Public Version
3
Public Version Date
2019-08-21
Public Version Status
Update
Public Device Record Key
7bcbd00e-1b44-405c-ac46-e1f377bbe24d

Device Description

CRILE FCP STR 5.5" STERL 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
GEN FORCEPS, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
61478 Surgical soft-tissue manipulation forceps, scissors-like, single-use

Identifiers

Type ID
Primary 50649111400801
Unit of Use 00649111400806