FDA UDI In Commercial Distribution 🇺🇸 United States

Myo Munchee

DI: 09359648000059 · Model: 1 · MYO MUNCHEE (OPERATIONS) PTY LTD
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Myo Munchee
Primary DI
09359648000059
Version / Model
1
Catalog Number
CB-SKIT-005
Company Name
MYO MUNCHEE (OPERATIONS) PTY LTD
Labeler DUNS
745300701
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-06
Public Version
1
Public Version Date
2024-06-14
Public Version Status
New
Public Device Record Key
48f6f0fd-a524-4e45-ba00-e4dc5e2e2b4e

Device Description

MYO MUNCHEE Sizing Kit Box 1 Piece

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Has Serial Number
No
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
ION Exerciser, Non-Measuring

GMDN Terms

Code Name
44858 Bite relief pad

Identifiers

Type ID
Primary 09359648000059
Package 09359648000066
Package 09359648000073

Customer Contacts

Phone
+61240775990