FDA UDI In Commercial Distribution 🇺🇸 United States

LARYNGEAL MIRROR

DI: 00192896097483 · Model: 502-249 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LARYNGEAL MIRROR
Primary DI
00192896097483
Version / Model
502-249
Catalog Number
502-249
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-06-06
Public Version
1
Public Version Date
2019-06-14
Public Version Status
New
Public Device Record Key
50b503ee-1263-4a1f-bf1d-2198dcb27fe1

Device Description

LARYNGEAL MIRROR WITH HANDLE #3

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
Yes
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
Yes
Sterilization Prior Use
Yes
Sterilization Methods
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
KAI Mirror, Ent

GMDN Terms

Code Name
33431 Laryngeal mirror, reusable

Identifiers

Type ID
Primary 00192896097483

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Length 12 Inch
Device Size Text, specify 20 Millimeter Tip