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Endoscopy Kit - Compliance

FDA UDI

Class I (US FDA UDI)

by Micro-tech Usa

Identity

Trade Name
Endoscopy Kit - Compliance FDA UDI
Generic Name
Endoscopy preparation kit FDA UDI
Device Name
Endoscopy Kit - Compliance FDA UDI
Model / Reference
KT1A0004A FDA UDI
Description
Endoscopy Kit - Compliance FDA UDI

Identifiers

Primary DI / UDI-DI
00850025860277 FDA UDI
FDA Product Code
KMJ FDA UDI
GMDN Term
Endoscopy preparation kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6375 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopy preparation kit

Endoscopy Kit - Compliance by Micro-tech Usa — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopy preparation kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Micro-tech Usa

Sources (1)

  • FDA UDI c1ef26b4-3aa7-42d9-8ddf-3bd63ea978b9 33 fields · synced May 30, 2026