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Ultrapower

FDA UDI

Class I (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
ULTRAPOWER FDA UDI
Generic Name
Orthopaedic bur, single-use FDA UDI
Device Name
ULTRAPOWER BUR, ROUND END (MUSTARD) 3.2 MM X 15.2 MM FDA UDI
Model / Reference
00702129400 FDA UDI
Description
ULTRAPOWER BUR, ROUND END (MUSTARD) 3.2 MM X 15.2 MM FDA UDI

Identifiers

Catalog Number
7021-294 FDA UDI
Primary DI / UDI-DI
10845854007532 FDA UDI
FDA Product Code
GFF FDA UDI
GMDN Term
Orthopaedic bur, 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
Outer Diameter — 3.2 Millimeter FDA UDI
Length — 15.2 Millimeter FDA UDI

Category: Orthopaedic bur, single-use

Ultrapower by Conmed Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bur, 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 6f1bdfe8-e7cd-4e01-85e2-8121dea43525 36 fields · synced May 31, 2026