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Conmed

FDA UDI

Class I (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CONMED FDA UDI
Generic Name
Endoscopic surgical probe FDA UDI
Device Name
MAXI-PROBE, STRAIGHT, 4.0 MM X 130 MM FDA UDI
Model / Reference
21.1002 FDA UDI
Description
MAXI-PROBE, STRAIGHT, 4.0 MM X 130 MM FDA UDI

Identifiers

Catalog Number
21.1002 FDA UDI
Primary DI / UDI-DI
10845854024409 FDA UDI
FDA Product Code
HXB FDA UDI
GMDN Term
Endoscopic surgical probe FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Dimensions & Sizes

Size
Width — 4 Millimeter FDA UDI
Length — 130 Millimeter FDA UDI

Category: Endoscopic surgical probe

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

Similar devices

Also classified as Endoscopic surgical probe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI c8941bed-b8fe-4bf2-bd97-236716a0a70a 36 fields · synced Jun 1, 2026