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Spacelabs Healthcare

FDA UDI

Class II (US FDA UDI)

by Spacelabs Healthcare (washington), Inc

Identity

Trade Name
Spacelabs Healthcare FDA UDI
Generic Name
Carbon dioxide absorber, reusable FDA UDI
Device Name
ABSORBER, NO BYPASS, 1KG (RE-ROUTE) FDA UDI
Model / Reference
Absorber FDA UDI
Description
ABSORBER, NO BYPASS, 1KG (RE-ROUTE) FDA UDI

Identifiers

Catalog Number
12200903 FDA UDI
Primary DI / UDI-DI
10841522100413 FDA UDI
FDA Product Code
CBK FDA UDI
GMDN Term
Carbon dioxide absorber, 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Carbon dioxide absorber, reusable

Spacelabs Healthcare by Spacelabs Healthcare (washington), Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Carbon dioxide absorber, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spacelabs Healthcare (washington), Inc

Sources (1)

  • FDA UDI 7d3cdaad-4524-4e6f-a32d-89293c075446 35 fields · synced Jun 7, 2026