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PhaSeal

FDA UDI

Class I (US FDA UDI)

by BD Switzerland Sàrl

Identity

Trade Name
PhaSeal FDA UDI
Generic Name
Ceiling-mounted intravenous hanger, single-use FDA UDI
Device Name
Hanger for IV-bag (M55) FDA UDI
Model / Reference
515405 FDA UDI
Description
Hanger for IV-bag (M55) FDA UDI

Identifiers

Catalog Number
515405 FDA UDI
Primary DI / UDI-DI
30382905154059 FDA UDI
FDA Product Code
FOX FDA UDI
GMDN Term
Ceiling-mounted intravenous hanger, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6990 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

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: Ceiling-mounted intravenous hanger, single-use

PhaSeal by BD Switzerland Sàrl — Class I — 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 4a554706-5105-4fac-ab61-d8f4012b079a 35 fields · synced May 30, 2026