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: General/plastic surgery mirror FDA UDI
Device Name: House Middle Ear Mirror, 2mm Diameter, Angled 45 Degrees, Round Handle, Overall Length 6.6" (168mm) FDA UDI
Model / Reference: 114-2816-67 FDA UDI
Description: House Middle Ear Mirror, 2mm Diameter, Angled 45 Degrees, Round Handle, Overall Length 6.6" (168mm) FDA UDI

Identifiers

Primary DI / UDI-DI: 00194613105877 FDA UDI
FDA Product Code: FTX FDA UDI
GMDN Term: General/plastic surgery mirror FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 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: General/plastic surgery mirror

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

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Symmetry Hardy — SYMMETRY SURGICAL INC. · Class I
MILLENNIUM — AVALIGN TECHNOLOGIES, Inc. · Class I
Mirror, round, polished — Spiggle & Theis Medizintechnik GmbH · Class I
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
Atticus mirror — Spiggle & Theis Medizintechnik GmbH · Class I

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 631f0957-47a1-4d3b-82a9-b392e0c9618e 34 fields · synced May 29, 2026