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Micro 100

FDA UDI

Class I (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
MICRO 100 FDA UDI
Generic Name
Foot-switch, pneumatic FDA UDI
Device Name
MICRO 100 FOOT CONTROL FDA UDI
Model / Reference
00137502800 FDA UDI
Description
MICRO 100 FOOT CONTROL FDA UDI

Identifiers

Catalog Number
1375-28 FDA UDI
Primary DI / UDI-DI
40845854022994 FDA UDI
FDA Product Code
HSZ FDA UDI
GMDN Term
Foot-switch, pneumatic 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

No

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Foot-switch, pneumatic

Micro 100 by Conmed Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foot-switch, pneumatic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 06c9ec1f-cec1-4f2b-8b91-942cf912c022 35 fields · synced May 30, 2026