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Gruber Cartilage Teflon Cutting Block

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Gruber Cartilage Teflon Cutting Block FDA UDI
Generic Name
Surgical cutting/shaping board, reusable FDA UDI
Device Name
Gruber Cartilage Teflon Cutting Block 120 Millimeter X 120 Millimeter X 15 Millimeter FDA UDI
Model / Reference
350-8453 FDA UDI
Description
Gruber Cartilage Teflon Cutting Block 120 Millimeter X 120 Millimeter X 15 Millimeter FDA UDI

Identifiers

Primary DI / UDI-DI
00192896105683 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

Category: Surgical cutting/shaping board, reusable

Gruber Cartilage Teflon 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 0c2ab9c1-c4b6-42d6-9b87-5efeee66cfd4 34 fields · synced Jun 8, 2026