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Reprocessed Micro Cut Dual Blade, 25 x 9mm

FDA UDI

Class I (US FDA UDI)

by Suretek Medical

Identity

Trade Name
Reprocessed Micro Cut Dual Blade, 25 x 9mm FDA UDI
Generic Name
Surgical power tool system handpiece, sawing, line-powered FDA UDI
Model / Reference
5400-3-111 FDA UDI

Identifiers

Primary DI / UDI-DI
B39054003111 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Surgical power tool system handpiece, sawing, line-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical power tool system handpiece, sawing, line-powered

Reprocessed Micro Cut Dual Blade, 25 x 9mm by Suretek Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical power tool system handpiece, sawing, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Suretek Medical

Sources (1)

  • FDA UDI 9258930e-0996-451a-b2b2-4d5258b396a4 32 fields · synced May 31, 2026