FDA UDI In Commercial Distribution 🇺🇸 United States

Blue Series - EF

DI: 00851861007024 · Model: SB030US · RESPIRE MEDICAL HOLDINGS LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Blue Series - EF
Primary DI
00851861007024
Version / Model
SB030US
Company Name
RESPIRE MEDICAL HOLDINGS LLC
Labeler DUNS
059636679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-20
Public Version
5
Public Version Date
2020-02-17
Public Version Status
Update
Public Device Record Key
8f55a0d5-ed8a-424f-b98c-9a95b2e57ba0

Device Description

Respire Blue Series EF

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
MR Conditional
Direct Marking Exempt
Yes
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 00851861007024

Customer Contacts

Phone
718-643-7326

Premarket Submissions

Submission Number Supplement Number
K152292 000

Device Sizes

Type Value Unit Text
Circumference 200 Millimeter