micsafe

FDA UDI

Class II (US FDA UDI)

by Jiangsu Micsafe Medical Tehcnology Co., LTD.

Identity

Trade Name: micsafe FDA UDI
Generic Name: ENFit oral/enteral syringe, single-use FDA UDI
Device Name: CAP FDA UDI
Model / Reference: 1 FDA UDI
Description: CAP FDA UDI

Identifiers

Primary DI / UDI-DI: 06971911292119 FDA UDI
FDA Product Code: PNR FDA UDI
GMDN Term: ENFit oral/enteral syringe, single-use 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: ENFit oral/enteral syringe, single-use

micsafe by Jiangsu Micsafe Medical Tehcnology Co., LTD. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

ENFit Syringe — Avanos Medical, Inc. · Class II
NeoMed Oral / Enteral Syringe — NEOMED, INC. · Class II
Health Care Logistics, Inc® — Health Care Logistics · Class I
NeoBottle — NEOMED, INC. · Class I
EXACTAMED — Baxter Healthcare Corp · Class I
Health Care Logistics, Inc® — Health Care Logistics · Class I
Ameritus Oral Syringe — KENTEC MEDICAL, INC. · Class I
VYGON — Vygon Corp. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Jiangsu Micsafe Medical Tehcnology Co., LTD.

Sources (1)

FDA UDI 0f3b3869-f715-413f-9802-13e61be2ce1c 33 fields · synced Jun 1, 2026