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: Intraocular retractor, single-use FDA UDI
Device Name: Premature Infant Self Retaining Retractor, Medium, Round Wire Blades, Blade Length Of 5mm, Overall Length 1-1/2" (38mm), Packed 1 Retractor Per Sterile Pouch, Disposable, 50 Per Package FDA UDI
Model / Reference: 5-54919S-DS FDA UDI
Description: Premature Infant Self Retaining Retractor, Medium, Round Wire Blades, Blade Length Of 5mm, Overall Length 1-1/2" (38mm), Packed 1 Retractor Per Sterile Pouch, Disposable, 50 Per Package FDA UDI

Identifiers

Primary DI / UDI-DI: 00194613010942 FDA UDI
FDA Product Code: HNI FDA UDI
GMDN Term: Intraocular retractor, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 886.4350 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Intraocular retractor, single-use

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 ac59ef7d-04d2-4413-92fb-61ff7351a2dc 34 fields · synced May 31, 2026