← Back to catalogue

Tricut

FDA UDI

Class I (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name
Tricut FDA UDI
Generic Name
Surgical saw blade, oscillating, single-use FDA UDI
Device Name
BLADE 1884080HR 5PK TRICUT M4 13CM 4MM FDA UDI
Model / Reference
1884080HR FDA UDI
Description
BLADE 1884080HR 5PK TRICUT M4 13CM 4MM FDA UDI

Identifiers

Primary DI / UDI-DI
20763000543826 FDA UDI
FDA Product Code
EQJ FDA UDI
GMDN Term
Surgical saw blade, oscillating, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4140 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 4.0 Millimeter FDA UDI
Length — 13.0 Centimeter FDA UDI

Category: Surgical saw blade, oscillating, single-use

Tricut by Medtronic Xomed, 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
Medtronic Xomed, Inc.

Sources (1)

  • FDA UDI 9bc8e0e2-ff1f-42b7-89d1-2d7e86dd63eb 35 fields · synced May 30, 2026