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Spray Catheter

FDA UDI

Class I (US FDA UDI)

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

Identity

Trade Name
Spray Catheter FDA UDI
Generic Name
Endoscopic spray catheter, single-use FDA UDI
Device Name
Blue handle 1.8mm OD 1600mm length FDA UDI
Model / Reference
WP-18/1600 FDA UDI
Description
Blue handle 1.8mm OD 1600mm length FDA UDI

Identifiers

Primary DI / UDI-DI
06932503562225 FDA UDI
FDA Product Code
GCE FDA UDI
GMDN Term
Endoscopic spray catheter, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Dimensions & Sizes

Size
Outer Diameter — 1.8 Millimeter FDA UDI
Length — 160 Centimeter FDA UDI

Category: Endoscopic spray catheter, single-use

Spray Catheter by Micro-Tech (Nanjing) Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic spray catheter, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0ce37ea8-f336-41be-a5de-3a5edace009f 35 fields · synced Jun 8, 2026