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Ferris Smith Rod Holder

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Ferris Smith Rod Holder FDA UDI
Generic Name
External orthopaedic fixation system, reusable FDA UDI
Device Name
Ferris Smith Rod Holder For 5.5 Millimeters Diameter Rods FDA UDI
Model / Reference
355-226 FDA UDI
Description
Ferris Smith Rod Holder For 5.5 Millimeters Diameter Rods FDA UDI

Identifiers

Primary DI / UDI-DI
00192896109391 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
External orthopaedic fixation system, reusable 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

Yes

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

Dimensions & Sizes

Size
Length — 7 Inch FDA UDI

Category: External orthopaedic fixation system, reusable

Ferris Smith Rod Holder by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External orthopaedic fixation system, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4f8b5f54-ac87-4d18-85de-19e1c978ed6c 35 fields · synced Jun 1, 2026