FDA UDI In Commercial Distribution 🇺🇸 United States

Sklar

DI: 50649111439788 · Model: 96-2239M · SKLAR CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
Sklar
Primary DI
50649111439788
Version / Model
96-2239M
Company Name
SKLAR CORPORATION
Labeler DUNS
006966006
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2019-03-20
Public Version
1
Public Version Date
2019-03-28
Public Version Status
New
Public Device Record Key
2d2fccd7-8d89-4bfe-a093-dc60fb36795d

Device Description

VIENNA NSL SPEC LG STRL 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
No
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
EPY SPECULUM, ENT

GMDN Terms

Code Name
42449 Nasal speculum, single-use

Identifiers

Type ID
Primary 50649111439788
Unit of Use 00649111439783