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Eco Magill

FDA UDI

Class I (US FDA UDI)

by Timesco Healthcare Limited

Identity

Trade Name
Eco Magill FDA UDI
Generic Name
Airway tube forceps, single-use FDA UDI
Device Name
Eco Magill Forceps Child 7.25" *single* FDA UDI
Model / Reference
D.04.200.21 FDA UDI
Description
Eco Magill Forceps Child 7.25" *single* FDA UDI

Identifiers

Primary DI / UDI-DI
05055382848783 FDA UDI
FDA Product Code
BWB FDA UDI
GMDN Term
Airway tube forceps, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5780 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

Category: Airway tube forceps, single-use

Eco Magill by Timesco Healthcare Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Airway tube forceps, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Timesco Healthcare Limited

Sources (1)

  • FDA UDI 792a272d-fb0d-48a9-966e-48022cbf7669 34 fields · synced Jun 8, 2026