← Back to catalogue

Jedmed

FDA UDI

Class II (US FDA UDI)

by JEDMED Instrument Company

Identity

Trade Name
JEDMED FDA UDI
Generic Name
Endoscope camera adaptor FDA UDI
Device Name
ETO CAP F/ERGOFLEX FDA UDI
Model / Reference
49-4985 FDA UDI
Description
ETO CAP F/ERGOFLEX FDA UDI

Identifiers

Catalog Number
49-4985 FDA UDI
Primary DI / UDI-DI
M6334949850 FDA UDI
FDA Product Code
EOB FDA UDI
GMDN Term
Endoscope camera adaptor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4760 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endoscope camera adaptor

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

Similar devices

Also classified as Endoscope camera adaptor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 7b220d37-fcb5-45da-b877-c0ad1fb52d00 34 fields · synced May 31, 2026