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Gastric Lavage Kit

FDA UDI

Class II (US FDA UDI)

by Mason Tayler Medical

Identity

Trade Name
Gastric Lavage Kit FDA UDI
Generic Name
Gastric lavage kit FDA UDI
Model / Reference
MTM5200 FDA UDI

Identifiers

Catalog Number
MTM5200 FDA UDI
Primary DI / UDI-DI
00860474000308 FDA UDI
FDA Product Code
KQT FDA UDI
GMDN Term
Gastric lavage kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4370 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Gastric lavage kit

Gastric Lavage Kit by Mason Tayler Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gastric lavage kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7beeffab-f2d2-4079-835b-b68558d8ff63 34 fields · synced Jun 1, 2026