FDA UDI In Commercial Distribution 🇺🇸 United States

TROUSSEAU TRACHEAL DILATOR RETRACTOR

DI: 00192896044173 · Model: 502-380 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TROUSSEAU TRACHEAL DILATOR RETRACTOR
Primary DI
00192896044173
Version / Model
502-380
Catalog Number
502-380
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
2
Public Version Date
2018-11-22
Public Version Status
Update
Public Device Record Key
ce0efd9e-d73f-4c1e-8011-4fcdfd53a808

Device Description

TROUSSEAU TRACHEAL DILATOR RETRACTOR ADOLESCENT MEDIUM SHAFT

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
KCG DILATOR, TRACHEAL

GMDN Terms

Code Name
11263 Tracheal surgery dilator, reusable

Identifiers

Type ID
Primary 00192896044173

Customer Contacts

Device Sizes

Type Value Unit Text
Length 5.25 Inch