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Global Healthcare

FDA UDI

Class II (US FDA UDI)

by Ghc Healthcare, Inc.

Identity

Trade Name
GLOBAL HEALTHCARE FDA UDI
Generic Name
Basic endotracheal tube, single-use FDA UDI
Device Name
ENDOTRACHEAL TUBE 6.5MM, CUFFED FDA UDI
Model / Reference
61-165 FDA UDI
Description
ENDOTRACHEAL TUBE 6.5MM, CUFFED FDA UDI

Identifiers

Primary DI / UDI-DI
00872237002566 FDA UDI
510(k) Number
K042683 FDA UDI
FDA Product Code
BTR FDA UDI
GMDN Term
Basic endotracheal tube, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5730 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Basic endotracheal tube, single-use

Global Healthcare by Ghc Healthcare, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic endotracheal tube, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2e043d26-34f0-4b28-8970-e886a29eff2f 34 fields · synced May 30, 2026