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Msi

FDA UDI

Class I (US FDA UDI)

by Modern Surgical Instruments LLC

Identity

Trade Name
MSI FDA UDI
Generic Name
Orthopaedic joint/limb rongeur FDA UDI
Device Name
Ortho Rongeur 10", FS Kerrison hdl, 7x16mm FDA UDI
Model / Reference
66.6707 FDA UDI
Description
Ortho Rongeur 10", FS Kerrison hdl, 7x16mm FDA UDI

Identifiers

Primary DI / UDI-DI
00810130204793 FDA UDI
FDA Product Code
HTX FDA UDI
GMDN Term
Orthopaedic joint/limb rongeur FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Orthopaedic joint/limb rongeur

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

Similar devices

Also classified as Orthopaedic joint/limb rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Modern Surgical Instruments LLC

Sources (1)

  • FDA UDI 1920095a-e0da-40a4-81fe-7a85c26c28bf 33 fields · synced May 31, 2026