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Jedmed

FDA UDI

Class I (US FDA UDI)

by JEDMED Instrument Company

Identity

Trade Name
JEDMED FDA UDI
Generic Name
ENT chair, electric FDA UDI
Device Name
"J-II" Chair JEDMED Motor Base 230V FDA UDI
Model / Reference
04-1557 FDA UDI
Description
"J-II" Chair JEDMED Motor Base 230V FDA UDI

Identifiers

Catalog Number
04-1557 FDA UDI
Primary DI / UDI-DI
M6330415570 FDA UDI
FDA Product Code
GBB FDA UDI
GMDN Term
ENT chair, electric FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: ENT chair, electric

Jedmed by JEDMED Instrument Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENT chair, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 47dcd74d-0f66-47d0-a3ae-14178ef2bea9 35 fields · synced May 30, 2026