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Msi

FDA UDI

Class II (US FDA UDI)

by Modern Surgical Instruments LLC

Identity

Trade Name
MSI FDA UDI
Generic Name
ENT suction dissector FDA UDI
Device Name
Frazier Suction Tube 7", 85mm WL, 8 french, 30deg with stylette FDA UDI
Model / Reference
75.9250 FDA UDI
Description
Frazier Suction Tube 7", 85mm WL, 8 french, 30deg with stylette FDA UDI

Identifiers

Primary DI / UDI-DI
00810130203420 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
ENT suction dissector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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: ENT suction dissector

Msi by Modern Surgical Instruments LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENT suction dissector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 915c3804-311f-4488-9b22-ca6425edc024 33 fields · synced May 30, 2026