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Endotracheal Tube with Evacuation Lumen

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref A01F01901FModel Standard Tracheal Tube HVLP cuffed: 3.0, 3.5, 4.0, 4.5, 5.0, 5.5, 6.0, 6.5, 7.0, 7.5, 8.0,18.5, 9.0, 9.5,10.0, 10.5, 11.0 mm

by Well Lead Medical Co., Ltd

Identity

Trade Name
Welllead Tracheal Tube with Evacuation Lumen EUDAMED
Endotracheal Tube with Evacuation Lumen FDA UDI
Generic Name
Basic endotracheal tube, single-use FDA UDI
Device Name
Tracheal Tube EUDAMED
PVC DEHP Free Cuff 9.0 FDA UDI
Model / Reference
A01F01901F EUDAMEDFDA UDI
Standard Tracheal Tube HVLP cuffed: 3.0, 3.5, 4.0, 4.5, 5.0, 5.5, 6.0, 6.5, 7.0, 7.5, 8.0,18.5, 9.0, 9.5,10.0, 10.5, 11.0 mm EUDAMED
Description
PVC DEHP Free Cuff 9.0 FDA UDI

Identifiers

Primary DI / UDI-DI
06944932774926 EUDAMEDFDA UDI
Basic UDI-DI
69449327FA01A00BW EUDAMED
510(k) Number
K182739 FDA UDI
FDA Product Code
BTR FDA UDI
EMDN Code
R01030201 ENDOTRACHEAL TUBES, CUFFED, NOT REINFORCED EUDAMED
GMDN Term
Basic endotracheal tube, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
868.5730 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Endotracheal Tube with Evacuation Lumen by Well Lead Medical Co., Ltd — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Basic endotracheal tube, single-use.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 71e708ec-5234-4375-9c2e-ed5cffcfbbc0 34 fields · synced Jul 21, 2026
  • EUDAMED 3ee1aab3-7cff-4ef2-8c30-e48f70898b3d 61 fields · synced Jul 21, 2026