FDA UDI In Commercial Distribution 🇺🇸 United States

Herbst Telescopic Flex

DI: 00851826007120 · Model: H1001 · SOMNOMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Herbst Telescopic Flex
Primary DI
00851826007120
Version / Model
H1001
Company Name
SOMNOMED, INC.
Labeler DUNS
623527962
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-14
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
2d1e3d1c-7c3f-439d-8a8d-df415f726113

Device Description

Oral Device For The Treatment Of Obstructive Sleep Apnea.

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
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LRK Device, Anti-Snoring

GMDN Terms

Code Name
47526 Mandible-repositioning sleep-disordered breathing orthosis

Identifiers

Type ID
Primary 00851826007120

Customer Contacts

Phone
888-447-6673

Premarket Submissions

Submission Number Supplement Number
K130558 000