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Diversatek Healthcare

FDA UDI

Class II (US FDA UDI)

by Diversatek Healthcare

Identity

Trade Name
Diversatek Healthcare FDA UDI
Generic Name
Endoscope channel support kit FDA UDI
Device Name
Fujifilm 5-pc Valve Kit FDA UDI
Model / Reference
1201-111 FDA UDI
Description
Fujifilm 5-pc Valve Kit FDA UDI

Identifiers

Catalog Number
1201-111 FDA UDI
Primary DI / UDI-DI
M78312011110 FDA UDI
FDA Product Code
OCX FDA UDI
ODC FDA UDI
FFY FDA UDI
GMDN Term
Endoscope channel support kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endoscope channel support kit

Diversatek Healthcare by Diversatek Healthcare — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope channel support kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5723a39d-af4c-40e2-b464-17424fa75e47 35 fields · synced May 31, 2026