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Hometa

FDA UDI

Class II (US FDA UDI)

by Hometa, Inc.

Identity

Trade Name
Hometa FDA UDI
Generic Name
Intravenous administration bag/bottle FDA UDI
Device Name
Empty EVA Bags 500mL FDA UDI
Model / Reference
60010 FDA UDI
Description
Empty EVA Bags 500mL FDA UDI

Identifiers

Primary DI / UDI-DI
00850024592025 FDA UDI
FDA Product Code
KPE FDA UDI
GMDN Term
Intravenous administration bag/bottle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5025 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: Intravenous administration bag/bottle

Hometa by Hometa, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravenous administration bag/bottle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hometa, Inc.

Sources (1)

  • FDA UDI 8568b991-3faa-4e51-acdf-e78c45386212 33 fields · synced May 30, 2026