← Back to catalogue

M-Catch

FDA UDI

Class I (US FDA UDI)

by Diversatek Healthcare

Identity

Trade Name
M-Catch FDA UDI
Generic Name
Gastrointestinal/airway foreign body retrieval basket, single-use FDA UDI
Device Name
Standard Retrieval Net, 3x6cm, 230cm FDA UDI
Model / Reference
1175-01 FDA UDI
Description
Standard Retrieval Net, 3x6cm, 230cm FDA UDI

Identifiers

Catalog Number
1175-01 FDA UDI
Primary DI / UDI-DI
00816734021361 FDA UDI
FDA Product Code
FGX FDA UDI
GMDN Term
Gastrointestinal/airway foreign body retrieval basket, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 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

Dimensions & Sizes

Size
Width — 3 Centimeter FDA UDI
Depth — 6 Centimeter FDA UDI
Length — 230 Centimeter FDA UDI

Category: Gastrointestinal/airway foreign body retrieval basket, single-use

M-Catch by Diversatek Healthcare — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gastrointestinal/airway foreign body retrieval basket, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Diversatek Healthcare

Sources (1)

  • FDA UDI 981eec73-f177-41a6-bb4d-16bce845a98a 37 fields · synced May 30, 2026