Astral Slimbag Bed Support

FDA UDI

Class II (US FDA UDI)

by Resmed Corp

Identity

Trade Name: Astral Slimbag Bed Support FDA UDI
Generic Name: Personal device holder, reusable FDA UDI
Device Name: Astral Slimbag Bed Support FDA UDI
Model / Reference: 27979 FDA UDI
Description: Astral Slimbag Bed Support FDA UDI

Identifiers

Catalog Number: 27979 FDA UDI
Primary DI / UDI-DI: 00619498279791 FDA UDI
FDA Product Code: CBK FDA UDI
GMDN Term: Personal device holder, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5895 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

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

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Personal device holder, reusable

Astral Slimbag Bed Support by Resmed Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Resmed Corp

Sources (1)

FDA UDI 3b02f9ce-0f8f-442f-89dc-4b54e74aef3d 35 fields · synced Jun 8, 2026