FDA UDI In Commercial Distribution 🇺🇸 United States

Amielle

DI: 00384702174017 · Model: SM 2174 · OWEN MUMFORD LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Amielle
Primary DI
00384702174017
Version / Model
SM 2174
Catalog Number
SM 2174
Company Name
OWEN MUMFORD LIMITED
Labeler DUNS
217266915
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-09-22
Public Version
4
Public Version Date
2021-07-01
Public Version Status
Update
Public Device Record Key
2cb4566c-011d-4e39-8921-734b0aeffd78

Device Description

Amielle Cone Size 4 is intended to be inserted into the vagina and progressively dilate the vagina

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KXP Stent, Vaginal

GMDN Terms

Code Name
11267 Vaginal dilator

Identifiers

Type ID
Primary 00384702174017
Unit of Use 00384702104007
Package 00384702174031

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K983045 000

Device Sizes

Type Value Unit Text
Length 160 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 40 Degrees Celsius