← Back to catalogue

Nasal Hood For Anesthesia Reusable Large

FDA UDI

Class I (US FDA UDI)

by Flexicare Medical Limited

Identity

Trade Name
Nasal Hood For Anesthesia Reusable Large FDA UDI
Generic Name
Anaesthesia face mask, reusable FDA UDI
Model / Reference
035-55-130U FDA UDI

Identifiers

Primary DI / UDI-DI
05055788753957 FDA UDI
FDA Product Code
KHA FDA UDI
GMDN Term
Anaesthesia face mask, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5590 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: Anaesthesia face mask, reusable

Nasal Hood For Anesthesia Reusable Large by Flexicare Medical Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia face mask, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI db7828c4-4d41-4584-9907-3d20a07f4374 32 fields · synced May 30, 2026