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B-Capta

FDA UDI

Class II (US FDA UDI)

by Sorin Group Italia Srl

Identity

Trade Name
B-CAPTA FDA UDI
Generic Name
Cardiopulmonary bypass system blood gas sensor FDA UDI
Model / Reference
1/4" VENOUS CUVETTE FDA UDI

Identifiers

Primary DI / UDI-DI
08033178113090 FDA UDI
510(k) Number
K202154 FDA UDI
FDA Product Code
DRY FDA UDI
GMDN Term
Cardiopulmonary bypass system blood gas sensor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4330 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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: Cardiopulmonary bypass system blood gas sensor

B-Capta by Sorin Group Italia Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiopulmonary bypass system blood gas sensor.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 51356e1a-4035-434a-9ed9-19cbc1cb2b66 33 fields · synced May 31, 2026