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Exactamed

FDA UDI

Class I (US FDA UDI)

by Baxter Healthcare Corp

Identity

Trade Name
EXACTAMED FDA UDI
Generic Name
ENFit oral/enteral syringe, single-use FDA UDI
Device Name
Oral Dispenser Clear 5 mL Pharmacy Pack FDA UDI
Model / Reference
H9387105 FDA UDI
Description
Oral Dispenser Clear 5 mL Pharmacy Pack FDA UDI

Identifiers

Catalog Number
H9387105 FDA UDI
Primary DI / UDI-DI
00085412478029 FDA UDI
FDA Product Code
KYX FDA UDI
GMDN Term
ENFit oral/enteral syringe, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6430 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

Dimensions & Sizes

Size
Total Volume — 5 Milliliter FDA UDI

Category: ENFit oral/enteral syringe, single-use

Exactamed by Baxter Healthcare Corp — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENFit oral/enteral syringe, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 810693fe-d2da-4f67-99ce-db8b98ad5b99 36 fields · synced May 29, 2026