FDA UDI In Commercial Distribution 🇺🇸 United States

Sklar®

DI: 40649111046972 · Model: 21-382 · SKLAR CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
12

Basic Information

Brand Name
Sklar®
Primary DI
40649111046972
Version / Model
21-382
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
1
Public Version Date
2018-09-10
Public Version Status
New
Public Device Record Key
9d552982-3684-4a89-b733-3a5e976f1e1b

Device Description

SIMPSON SOUND W/CM 12.5" 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
FBX SOUND, URETHRAL, METAL OR PLASTIC

GMDN Terms

Code Name
46435 Uterine sound, single-use

Identifiers

Type ID
Primary 40649111046972
Unit of Use 00649111046974