FDA UDI In Commercial Distribution 🇺🇸 United States

Sklar

DI: 10649111444173 · Model: 49-8602 · SKLAR CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sklar
Primary DI
10649111444173
Version / Model
49-8602
Company Name
SKLAR CORPORATION
Labeler DUNS
006966006
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-08
Public Version
2
Public Version Date
2020-12-04
Public Version Status
Update
Public Device Record Key
b0065d06-401c-4be7-a11d-27e0b113589c

Device Description

WINTER ROOT ELEVATOR 11L

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
EMJ ELEVATOR, SURGICAL, DENTAL

GMDN Terms

Code Name
38168 Periosteal elevator, reusable

Identifiers

Type ID
Primary 10649111444173