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Accu-Cut® SRM™ 200

FDA UDI

Class I (US FDA UDI)

by Sakura Finetek USA, Inc

Identity

Trade Name
Accu-Cut® SRM™ 200 FDA UDI
Generic Name
Rotary microtome IVD FDA UDI
Device Name
Rotary Microtome (Retracting) FDA UDI
Model / Reference
1429 FDA UDI
Description
Rotary Microtome (Retracting) FDA UDI

Identifiers

Catalog Number
1429 FDA UDI
Primary DI / UDI-DI
08720177655170 FDA UDI
FDA Product Code
IDO FDA UDI
GMDN Term
Rotary microtome IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3010 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Rotary microtome IVD

Accu-Cut® SRM™ 200 by Sakura Finetek USA, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rotary microtome IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f6b02f0c-e9af-4faf-ac22-cc1d1fddd75d 35 fields · synced May 30, 2026