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Ventilation

FDA UDI

Class I (US FDA UDI)

by Sarstedt Aktiengesellschaft & Co.KG

Identity

Trade Name
Ventilation FDA UDI
Generic Name
Blood gas syringe IVD, lithium heparin FDA UDI
Device Name
Ventilation for blood gas Monovette FDA UDI
Model / Reference
14.1148 FDA UDI
Description
Ventilation for blood gas Monovette FDA UDI

Identifiers

Catalog Number
14.1148 FDA UDI
Primary DI / UDI-DI
04038917085465 FDA UDI
FDA Product Code
JRC FDA UDI
GMDN Term
Blood gas syringe IVD, lithium heparin FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood gas syringe IVD, lithium heparin

Ventilation by Sarstedt Aktiengesellschaft & Co.KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood gas syringe IVD, lithium heparin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ed6c7c65-940b-4a62-9258-be10976df5a3 35 fields · synced May 30, 2026