← Back to catalogue

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, oscillating, single-use FDA UDI
Device Name
Blade, Osc. Wedge Cut 2mm FDA UDI
Model / Reference
BO1027B2N FDA UDI
Description
Blade, Osc. Wedge Cut 2mm FDA UDI

Identifiers

Catalog Number
BO1027B2N FDA UDI
Primary DI / UDI-DI
00841731118363 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Surgical saw blade, oscillating, 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, oscillating, 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, oscillating, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Vilex In Tennessee, Inc.

Sources (1)

  • FDA UDI 215d4ad5-f657-477b-b7cf-3d977cde0296 34 fields · synced Jun 8, 2026