MSI Precision Specialty Instruments

FDA UDI

Class I (US FDA UDI)

by Med Saver, Inc.

Identity

Trade Name: MSI Precision Specialty Instruments FDA UDI
Generic Name: Vaginal speculum, reusable FDA UDI
Device Name: Laser Specula, Large, Laser, Inner Blades Are Matte Finish, External Blades Are Polished Stainless Steel, One Smoke Evacuation Tube On Upper Blade FDA UDI
Model / Reference: 619725PIL FDA UDI
Description: Laser Specula, Large, Laser, Inner Blades Are Matte Finish, External Blades Are Polished Stainless Steel, One Smoke Evacuation Tube On Upper Blade FDA UDI

Identifiers

Primary DI / UDI-DI: 00194613033408 FDA UDI
FDA Product Code: HDF FDA UDI
GMDN Term: Vaginal speculum, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 884.4520 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Vaginal speculum, reusable

MSI Precision Specialty Instruments by Med Saver, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Med Saver, Inc.

Sources (1)

FDA UDI f7558e13-7c77-445a-8e27-e67538dbf9ca 34 fields · synced May 31, 2026