Preparation tray, stainless steel

FDA UDI

Class I (US FDA UDI)

by Spiggle & Theis Medizintechnik GmbH

Identity

Trade Name: Preparation tray, stainless steel FDA UDI
Generic Name: Surgical cutting/shaping board, reusable FDA UDI
Device Name: with scale, 92x54 mm FDA UDI
Model / Reference: 10-735-00 FDA UDI
Description: with scale, 92x54 mm FDA UDI

Identifiers

Catalog Number: 10-735-00 FDA UDI
Primary DI / UDI-DI: 04250381850169 FDA UDI
FDA Product Code: NNR FDA UDI
GMDN Term: Surgical cutting/shaping board, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 874.3540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Surgical cutting/shaping board, reusable

Preparation tray, stainless steel by Spiggle & Theis Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical cutting/shaping board, reusable.

Tissue-Tek® Accu-Edge® — Sakura Finetek USA, Inc · Class I
MSI Precision Specialty Instruments — Med Saver, Inc. · Class I
MILLENNIUM — AVALIGN TECHNOLOGIES, Inc. · Class I
Marina Medical — MARINA MEDICAL INSTRUMENTS, INC. · Class I
Gyrus ACMI — Gyrus Acmi, Inc. · Class I
V. Mueller — STERIS CORPORATION · Class I
Graft Processing Board — COLE INSTRUMENTS · Class I
MILLENNIUM — AVALIGN TECHNOLOGIES, Inc. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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

Manufacturer

Manufacturer: Spiggle & Theis Medizintechnik GmbH

Sources (1)

FDA UDI 75b8263a-3054-45db-bc99-cd24d94fb64f 35 fields · synced Jun 1, 2026