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Teflon Cartilage Cutting Block

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
TEFLON CARTILAGE CUTTING BLOCK FDA UDI
Generic Name
Surgical cutting/shaping board, reusable FDA UDI
Device Name
TEFLON CARTILAGE CUTTING BLOCK FDA UDI
Model / Reference
350-8451 FDA UDI
Description
TEFLON CARTILAGE CUTTING BLOCK FDA UDI

Identifiers

Catalog Number
350-8451 FDA UDI
Primary DI / UDI-DI
00192896032026 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Surgical cutting/shaping board, 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

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

Dimensions & Sizes

Size
Length — 85 Millimeter FDA UDI
Width — 55 Millimeter FDA UDI
Height — 10 Millimeter FDA UDI

Category: Surgical cutting/shaping board, reusable

Teflon Cartilage Cutting Block by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical cutting/shaping board, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fc572e18-fdfe-446c-8bf8-0fbfddb8a473 36 fields · synced May 30, 2026