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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
Bone curette, reusable FDA UDI
Device Name
Long Cobb Elevator 15" Overall With 9" Handle, 3/4" Width FDA UDI
Model / Reference
90-0125 FDA UDI
Description
Long Cobb Elevator 15" Overall With 9" Handle, 3/4" Width FDA UDI

Identifiers

Primary DI / UDI-DI
00810130205837 FDA UDI
FDA Product Code
FZS FDA UDI
GMDN Term
Bone curette, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Bone curette, reusable

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

Similar devices

Also classified as Bone curette, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 38d7442b-28c1-41b4-a9f1-6455d7232935 33 fields · synced May 31, 2026