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Reli®

FDA UDI

Class II (US FDA UDI)

by Myco Medical Supplies Inc.

Identity

Trade Name
RELI® FDA UDI
Generic Name
Hypodermic needle, single-use FDA UDI
Device Name
Safety Hypodermic Needle with Syringe, Low Dead Space, 3ml, 23G x 1" FDA UDI
Model / Reference
SHN23G101-S3ML-LDS FDA UDI
Description
Safety Hypodermic Needle with Syringe, Low Dead Space, 3ml, 23G x 1" FDA UDI

Identifiers

Catalog Number
SHN23G101-S3ML-LDS FDA UDI
Primary DI / UDI-DI
00386120011707 FDA UDI
FDA Product Code
FMI FDA UDI
MEG FDA UDI
FMF FDA UDI
GMDN Term
Hypodermic needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 FDA UDI
880.5860 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

Dimensions & Sizes

Size
Total Volume — 3 Milliliter FDA UDI
Needle Gauge — 23 Gauge FDA UDI
Length — 1 Inch FDA UDI

Category: Hypodermic needle, single-use

Reli® by Myco Medical Supplies Inc. — 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 9eaf7071-fb17-41cd-9731-e9474dcac72e 35 fields · synced May 31, 2026