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DJF Med

FDA UDI

Class II (US FDA UDI)

by Acta Medical LLC

Identity

Trade Name
DJF Med FDA UDI
Generic Name
Intravenous administration bag/bottle FDA UDI
Device Name
1000ml Enteral Feeding Set FDA UDI
Model / Reference
DJF1000J FDA UDI
Description
1000ml Enteral Feeding Set FDA UDI

Identifiers

Primary DI / UDI-DI
00850033629293 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Intravenous administration bag/bottle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 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

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

DJF Med by Acta Medical LLC — 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
Acta Medical LLC

Sources (1)

  • FDA UDI 38321ba2-3867-49d6-8f13-99b5e3406dad 33 fields · synced Jun 1, 2026