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UNICO ColpoMaster III

FDA UDI

Class II (US FDA UDI)

by United Products & Instruments, Inc.

Identity

Trade Name
UNICO ColpoMaster III FDA UDI
Generic Name
Colposcope FDA UDI
Device Name
CS-305 Colposcope Center Post, Triple Magnification, Five Legged Base. LED Illumination. FDA UDI
Model / Reference
CS-305 FDA UDI
Description
CS-305 Colposcope Center Post, Triple Magnification, Five Legged Base. LED Illumination. FDA UDI

Identifiers

Catalog Number
CS-305 FDA UDI
Primary DI / UDI-DI
00816668020089 FDA UDI
510(k) Number
K073053 FDA UDI
FDA Product Code
HEX FDA UDI
GMDN Term
Colposcope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1630 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Colposcope

UNICO ColpoMaster III by United Products & Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Colposcope.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b41ae84a-d2fd-4e3a-884e-399b329e5900 36 fields · synced May 30, 2026