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Jedmed

FDA UDI

Class II (US FDA UDI)

by JEDMED Instrument Company

Identity

Trade Name
JEDMED FDA UDI
Generic Name
Camera control unit FDA UDI
Device Name
EYECUP SLEEVE F/HORUS SCOPE FDA UDI
Model / Reference
39-7439 FDA UDI
Description
EYECUP SLEEVE F/HORUS SCOPE FDA UDI

Identifiers

Catalog Number
39-7439 FDA UDI
Primary DI / UDI-DI
M6333974390 FDA UDI
510(k) Number
K120982 FDA UDI
FDA Product Code
HKI FDA UDI
GMDN Term
Camera control unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1120 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: Camera control unit

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

Similar devices

Also classified as Camera control unit.

Cleared under the same submission

K120982 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
JEDMED Instrument Company

Sources (1)

  • FDA UDI 97e3a23c-52cc-4e2e-b59e-c201ae067d8f 35 fields · synced May 31, 2026