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Amielle

FDA UDI

Class II (US FDA UDI)

by Owen Mumford Usa Incorporated

Identity

Trade Name
Amielle FDA UDI
Generic Name
Vaginal dilator FDA UDI
Device Name
Amielle cone size 1 FDA UDI
Model / Reference
SM 2102 FDA UDI
Description
Amielle cone size 1 FDA UDI

Identifiers

Catalog Number
SM 2102 FDA UDI
Primary DI / UDI-DI
00384702102010 FDA UDI
510(k) Number
K983045 FDA UDI
FDA Product Code
KXP FDA UDI
GMDN Term
Vaginal dilator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.3900 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 89 Millimeter FDA UDI

Category: Vaginal dilator

Amielle by Owen Mumford Usa Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vaginal dilator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cd188859-bbb2-4ac2-9a70-4572f0ac5e2b 38 fields · synced May 30, 2026