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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 scissors, reusable FDA UDI
Device Name
Troutman-Castroviejo Corneal Section Scissors, Left, Barraquer Stop/Lock, Miniature Model Has Curved Blades, Blunt Tips, Both Blades Of Equal Length, 13mm Mid-Screw To Tip, Overall Length 4-1/8" (105mm) FDA UDI
Model / Reference
5-4422 FDA UDI
Description
Troutman-Castroviejo Corneal Section Scissors, Left, Barraquer Stop/Lock, Miniature Model Has Curved Blades, Blunt Tips, Both Blades Of Equal Length, 13mm Mid-Screw To Tip, Overall Length 4-1/8" (105mm) FDA UDI

Identifiers

Primary DI / UDI-DI
00194613076320 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Corneal scissors, reusable 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

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Corneal scissors, reusable

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

Similar devices

Also classified as Corneal scissors, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Med Saver, Inc.

Sources (1)

  • FDA UDI 0cf0d762-3321-432a-aa31-5282c2bde8ff 34 fields · synced Jun 6, 2026