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Unimed

FDA UDI

Class II (US FDA UDI)

by Unimed Medical Supplies, Inc.

Identity

Trade Name
Unimed FDA UDI
Generic Name
Rigid optical cystourethroscope FDA UDI
Device Name
One piece ECG monitor cable/Philips/5-lead/grabber/AHA/2.5M+0.9M/020 FDA UDI
Model / Reference
25029P FDA UDI
Description
One piece ECG monitor cable/Philips/5-lead/grabber/AHA/2.5M+0.9M/020 FDA UDI

Identifiers

Primary DI / UDI-DI
06945664845885 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Rigid optical cystourethroscope 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Rigid optical cystourethroscope

Unimed by Unimed Medical Supplies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid optical cystourethroscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Unimed Medical Supplies, Inc.

Sources (1)

  • FDA UDI bc65323f-7a91-4c89-885f-44d505248cdd 33 fields · synced May 30, 2026