FDA UDI In Commercial Distribution 🇺🇸 United States

JACKSON TRACHEAL RETRACTOR

DI: 00192896044210 · Model: 502-399 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
JACKSON TRACHEAL RETRACTOR
Primary DI
00192896044210
Version / Model
502-399
Catalog Number
502-399
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-14
Public Version
1
Public Version Date
2018-10-15
Public Version Status
New
Public Device Record Key
b5c372cb-5d07-4e0e-ac2f-c0aa4257ffb8

Device Description

JACKSON TRACHEAL RETRACTOR

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
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", "Dry Heat Sterilization"]

Product Codes

Code Name
KAL RETRACTOR, ENT

GMDN Terms

Code Name
35112 Tracheal hook

Identifiers

Type ID
Primary 00192896044210

Customer Contacts

Device Sizes

Type Value Unit Text
Length 7 Inch