FDA UDI In Commercial Distribution 🇺🇸 United States

EMA

DI: 90842326101008 · Model: EMAST13WSB · The Myerson Company Limited
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EMA
Primary DI
90842326101008
Version / Model
EMAST13WSB
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
4e7ee9ad-e6da-4839-ad93-6b086cfd746c

Device Description

EMA Strap 13mm White/Soft Bulk

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
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 90842326101008

Customer Contacts

Phone
18004232683

Premarket Submissions

Submission Number Supplement Number
K971794 000

Device Sizes

Type Value Unit Text
Length 13 Millimeter