SE CHILD RESUSCITATOR BALL 500ML W/ MDI PORT , 40cm H2O&MANOMETER PORT

FDA UDI

Class II (US FDA UDI)

by Besmed Health Business Corp.

Identity

Trade Name: SE CHILD RESUSCITATOR BALL 500ML W/ MDI PORT , 40cm H2O&MANOMETER PORT FDA UDI
Generic Name: Pulmonary resuscitator, manual, reusable FDA UDI
Device Name: SE CHILD RESUSCITATOR BALL 500ML W/ MDI PORT , 40cm H2O&MANOMETER PORT FDA UDI
Model / Reference: RE-24531 FDA UDI
Description: SE CHILD RESUSCITATOR BALL 500ML W/ MDI PORT , 40cm H2O&MANOMETER PORT FDA UDI

Identifiers

Primary DI / UDI-DI: 04716770245317 FDA UDI
FDA Product Code: BTM FDA UDI
GMDN Term: Pulmonary resuscitator, manual, reusable 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pulmonary resuscitator, manual, reusable

SE CHILD RESUSCITATOR BALL 500ML W/ MDI PORT , 40cm H2O&MANOMETER PORT by Besmed Health Business Corp. — Class II — FDA UDI — listed in FDA GUDID

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Besmed Health Business Corp.

Sources (1)

FDA UDI a724bd59-e4a3-4174-ba9d-2411f65796b7 33 fields · synced May 30, 2026