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Conmed

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CONMED FDA UDI
Generic Name
Bariatric bed FDA UDI
Device Name
Radiotranslucent D Series 48 Inch Leadwire FDA UDI
Model / Reference
RTD48-05 FDA UDI
Description
Radiotranslucent D Series 48 Inch Leadwire FDA UDI

Identifiers

Catalog Number
RTD48-05 FDA UDI
Primary DI / UDI-DI
30653405002851 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Bariatric bed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2900 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Bariatric bed

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

Similar devices

Also classified as Bariatric bed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI c88718f4-34d6-47e7-8bec-c3e0257322c9 36 fields · synced Jun 6, 2026