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Alaris, VersaSafe

FDA UDI

Class II (US FDA UDI)

by BD Switzerland Sàrl

Identity

Trade Name
Alaris, VersaSafe FDA UDI
Generic Name
Blood transfusion set, non-exchange FDA UDI
Device Name
GRAV BLD SET NV DP W/180 MC FLTR 2VS FDA UDI
Model / Reference
420800E-07 FDA UDI
Description
GRAV BLD SET NV DP W/180 MC FLTR 2VS FDA UDI

Identifiers

Catalog Number
420800E-07 FDA UDI
Primary DI / UDI-DI
10885403220586 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Blood transfusion set, non-exchange FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 FDA UDI
Commercial Distribution
Not 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

Alaris, VersaSafe by BD Switzerland Sàrl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6984aa54-54df-4bfe-8219-fd0e0f67b6da 36 fields · synced Jun 1, 2026