FDA UDI In Commercial Distribution 🇺🇸 United States

EMA

DI: 00842326100534 · Model: EMAKT12008 · The Myerson Company Limited
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EMA
Primary DI
00842326100534
Version / Model
EMAKT12008
Company Name
The Myerson Company Limited
Labeler DUNS
857278431
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2019-12-09
Public Version Status
Update
Public Device Record Key
1e001a90-290e-4965-a7bf-6cf518b7b1a8

Device Description

EMA Kit3 with 120mmx2.0mm disc

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
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
No

Product Codes

Code Name
LRK Device, Anti-Snoring

GMDN Terms

Code Name
47526 Mandible-repositioning sleep-disordered breathing orthosis

Identifiers

Type ID
Primary 00842326100534

Customer Contacts

Phone
18004232683

Premarket Submissions

Submission Number Supplement Number
K971794 000

Device Sizes

Type Value Unit Text
Height 2.0 Millimeter
Outer Diameter 120 Millimeter