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AMSure® Disposable Vaginal Speculum

FDA UDI

Class II (US FDA UDI)

by Amsino International, Inc.

Identity

Trade Name
AMSure® Disposable Vaginal Speculum FDA UDI
Generic Name
Vaginal speculum, single-use FDA UDI
Device Name
AMSure® Disposable Vaginal Speculum Graves Style, Clean, Ready For Use FDA UDI
Model / Reference
1 FDA UDI
Description
AMSure® Disposable Vaginal Speculum Graves Style, Clean, Ready For Use FDA UDI

Identifiers

Catalog Number
AS032M FDA UDI
Primary DI / UDI-DI
10704411002260 FDA UDI
FDA Product Code
HIB FDA UDI
GMDN Term
Vaginal speculum, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4530 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vaginal speculum, single-use

AMSure® Disposable Vaginal Speculum by Amsino International, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vaginal speculum, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dc97dc92-54c4-4f53-8b3e-2c28faae36e7 34 fields · synced May 29, 2026