← Back to catalogue

Msi

FDA UDI

Class I (US FDA UDI)

by Modern Surgical Instruments LLC

Identity

Trade Name
MSI FDA UDI
Generic Name
Skull clamp FDA UDI
Device Name
MF-Adjustable Base Unit with connecting arm FDA UDI
Model / Reference
17-0015 FDA UDI
Description
MF-Adjustable Base Unit with connecting arm FDA UDI

Identifiers

Primary DI / UDI-DI
00810130203826 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Skull clamp 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: Skull clamp

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

Similar devices

Also classified as Skull clamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 3e2462d3-3ff6-4c39-b1a0-1e313d39b6c7 33 fields · synced May 30, 2026