SpiraLith Ca

FDA UDI

Class I (US FDA UDI)

by Micropore Inc

Identity

Trade Name: SpiraLith Ca FDA UDI
Generic Name: Carbon dioxide absorber, single-use FDA UDI
Model / Reference: Rx-3903C FDA UDI

Identifiers

Primary DI / UDI-DI: 00860008449849 FDA UDI
FDA Product Code: CBL FDA UDI
GMDN Term: Carbon dioxide absorber, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5300 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

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Carbon dioxide absorber, single-use

SpiraLith Ca by Micropore Inc — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Micropore Inc

Sources (1)

FDA UDI 95f3c694-6b73-4c6d-8c52-d22338b38920 32 fields · synced May 30, 2026