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Mimix, STEALTH

FDA UDI

Class I (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
Mimix, STEALTH FDA UDI
Generic Name
Arthroscopic shaver system blade, single-use FDA UDI
Device Name
MIMIX 35° FRR STEALTH, 2.9 MM FDA UDI
Model / Reference
LE-29FRP FDA UDI
Description
MIMIX 35° FRR STEALTH, 2.9 MM FDA UDI

Identifiers

Catalog Number
LE-29FRP FDA UDI
Primary DI / UDI-DI
20845854649180 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Arthroscopic shaver system blade, 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

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

Dimensions & Sizes

Size
Length — 2.9 Millimeter FDA UDI
Angle — 35 degree FDA UDI

Category: Arthroscopic shaver system blade, single-use

Mimix, STEALTH by Conmed Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic shaver system blade, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 55097dbd-2762-43cb-9ee6-581f03701602 37 fields · synced Jun 1, 2026