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Evotech

FDA UDI

Class II (US FDA UDI)

by Advanced Sterilization Products Services Inc.

Identity

Trade Name
Evotech FDA UDI
Generic Name
Endoscope channel-opening adaptor FDA UDI
Device Name
Channel Connector Tube, Brown FDA UDI
Model / Reference
104502 FDA UDI
Description
Channel Connector Tube, Brown FDA UDI

Identifiers

Catalog Number
104502 FDA UDI
Primary DI / UDI-DI
10705037049455 FDA UDI
510(k) Number
K082392 FDA UDI
K140977 FDA UDI
FDA Product Code
FEB FDA UDI
GMDN Term
Endoscope channel-opening adaptor 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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: Endoscope channel-opening adaptor

Evotech by Advanced Sterilization Products Services Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope channel-opening adaptor.

Cleared under the same submission

K082392 also covers:

K140977 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Advanced Sterilization Products Services Inc.

Sources (1)

  • FDA UDI 2aa1db4c-f0a4-4111-9902-d4f7a581fd04 37 fields · synced Jun 7, 2026