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Vilex Power Accessory

FDA UDI

Class I (US FDA UDI)

by Vilex In Tennessee, Inc.

Identity

Trade Name
Vilex Power Accessory FDA UDI
Generic Name
Surgical saw blade, sagittal, single-use FDA UDI
Device Name
Blade, Sag. 4. 5x 25.5mm Fine FDA UDI
Model / Reference
BS4525FN FDA UDI
Description
Blade, Sag. 4. 5x 25.5mm Fine FDA UDI

Identifiers

Catalog Number
BS4525FN FDA UDI
Primary DI / UDI-DI
00841731118493 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Surgical saw blade, sagittal, single-use 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical saw blade, sagittal, single-use

Vilex Power Accessory by Vilex In Tennessee, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical saw blade, sagittal, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 625ee80b-f636-4825-8f21-41b1291ce825 34 fields · synced May 30, 2026