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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
Surgical implant/trial-implant/sizer holder, reusable FDA UDI
Device Name
SL Bone Graft Holder total length 21,6 cm FDA UDI
Model / Reference
18-5040 FDA UDI
Description
SL Bone Graft Holder total length 21,6 cm FDA UDI

Identifiers

Primary DI / UDI-DI
00810130204229 FDA UDI
FDA Product Code
GEN FDA UDI
GMDN Term
Surgical implant/trial-implant/sizer holder, 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: Surgical implant/trial-implant/sizer holder, reusable

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

Similar devices

Also classified as Surgical implant/trial-implant/sizer holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 00f86e49-2bc8-493f-b566-ab1c7222a6b3 33 fields · synced May 30, 2026