Hand Pump Assembly

FDA UDI

Class II (US FDA UDI)

by Mercury Enterprises, Inc.

Identity

Trade Name: Hand Pump Assembly FDA UDI
Generic Name: Gastric calibration tube FDA UDI
Model / Reference: 88-GCT501 FDA UDI

Identifiers

Primary DI / UDI-DI: 10641043885017 FDA UDI
510(k) Number: K222880 FDA UDI
FDA Product Code: KNT FDA UDI
GMDN Term: Gastric calibration tube FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.5980 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Gastric calibration tube

Hand Pump Assembly by Mercury Enterprises, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Mercury Enterprises, Inc.

Sources (1)

FDA UDI 1a6aebbd-dfcf-45f4-835a-00bfcb255d3d 34 fields · synced May 30, 2026