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CatchAll(TM) Transport Pad

FDA UDI

Class I (US FDA UDI)

by Micro-Tech (Nanjing) Co., Ltd.

Identity

Trade Name
CatchAll(TM) Transport Pad FDA UDI
Generic Name
Endoscopy preparation kit FDA UDI
Device Name
blue,25 pcs per PE bag,,25 pcs per case box,4 case boxes per carton FDA UDI
Model / Reference
CTP-02025 FDA UDI
Description
blue,25 pcs per PE bag,,25 pcs per case box,4 case boxes per carton FDA UDI

Identifiers

Primary DI / UDI-DI
06932503562133 FDA UDI
FDA Product Code
KME FDA UDI
GMDN Term
Endoscopy preparation kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6060 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

No

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

No

FDA UDI

Category: Endoscopy preparation kit

CatchAll(TM) Transport Pad by Micro-Tech (Nanjing) Co., Ltd. — 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 (Nanjing) Co., Ltd.

Sources (1)

  • FDA UDI d808afb9-e089-4fe1-98f9-a933e403b5ce 34 fields · synced May 30, 2026