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Micsafe

FDA UDI

Class II (US FDA UDI)

by Jiangsu Micsafe Medical Tehcnology Co., LTD.

Identity

Trade Name
Micsafe FDA UDI
Generic Name
Hypodermic needle, single-use FDA UDI
Device Name
Safety Needle 25G*1.5'' FDA UDI
Model / Reference
1 FDA UDI
Description
Safety Needle 25G*1.5'' FDA UDI

Identifiers

Primary DI / UDI-DI
06971911290382 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Hypodermic needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 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: Hypodermic needle, 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 Hypodermic needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cc982277-3845-4852-b74d-36047acb8f4f 33 fields · synced Jun 8, 2026