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: Corneal marker, reusable FDA UDI
Device Name: Toric Intra-Op Axis Marker II Degreega, Titanium, Two 2mm Marking Blades, Cutouts On Two 180 Degrees Positions For Easy Alignment, Markings Every 10 Degrees, Mounted At 90 Degrees Position, Round Handle FDA UDI
Model / Reference: 15-3805TAS FDA UDI
Description: Toric Intra-Op Axis Marker II Degreega, Titanium, Two 2mm Marking Blades, Cutouts On Two 180 Degrees Positions For Easy Alignment, Markings Every 10 Degrees, Mounted At 90 Degrees Position, Round Handle FDA UDI

Identifiers

Primary DI / UDI-DI: 00194613106256 FDA UDI
FDA Product Code: HMR FDA UDI
GMDN Term: Corneal marker, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 886.4570 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

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Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

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Lot / Batch Number

Yes

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Serial Number

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Expiration Date

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Manufacturing Date

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Corneal marker, 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 085509b3-5598-45c0-b958-e4b24ef2152f 34 fields · synced Jun 1, 2026