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Flexicare

FDA UDI

Class II (US FDA UDI)

by Flexicare Medical Limited

Identity

Trade Name
Flexicare FDA UDI
Generic Name
Pulmonary resuscitator, manual, single-use FDA UDI
Device Name
Adult Single Use Resuscitator + Strap + Pressure Relief 60cmH20 + Mask Size 5 + M/MS 10ft line FDA UDI
Model / Reference
038-71-940/1U FDA UDI
Description
Adult Single Use Resuscitator + Strap + Pressure Relief 60cmH20 + Mask Size 5 + M/MS 10ft line FDA UDI

Identifiers

Primary DI / UDI-DI
05055931117896 FDA UDI
FDA Product Code
BTM FDA UDI
GMDN Term
Pulmonary resuscitator, manual, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5915 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pulmonary resuscitator, manual, single-use

Flexicare by Flexicare Medical Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary resuscitator, manual, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 385f8f6f-6dc0-4070-b343-1f84c7eb9eaa 33 fields · synced May 31, 2026