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Ntersurgical Ecolite, Paediatric, Medium Concentration Oxygen Mask And Tube

FDA UDI

Class I (US FDA UDI)

by Intersurgical Incorporated

Identity

Trade Name
NTERSURGICAL ECOLITE, PAEDIATRIC, MEDIUM CONCENTRATION OXYGEN MASK AND TUBE FDA UDI
Generic Name
Rebreathing oxygen face mask FDA UDI
Device Name
NTERSURGICAL ECOLITE, PAEDIATRIC, MEDIUM CONCENTRATION OXYGEN MASK AND TUBE WITH UNIVERSAL CONNECTOR, 2.1M FDA UDI
Model / Reference
1196019 FDA UDI
Description
NTERSURGICAL ECOLITE, PAEDIATRIC, MEDIUM CONCENTRATION OXYGEN MASK AND TUBE WITH UNIVERSAL CONNECTOR, 2.1M FDA UDI

Identifiers

Primary DI / UDI-DI
05030267157860 FDA UDI
FDA Product Code
BYG FDA UDI
GMDN Term
Rebreathing oxygen face mask FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5580 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

Yes

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: Rebreathing oxygen face mask

Ntersurgical Ecolite, Paediatric, Medium Concentration Oxygen Mask And Tube by Intersurgical Incorporated — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Rebreathing oxygen face mask.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dc60f8ee-d912-4c30-8015-683a9ab1b1a0 34 fields · synced Jun 8, 2026