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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
General-purpose syringe/needle FDA UDI
Device Name
Reli® Syringe, 10ML, 100ea/bx, 15bx/cs FDA UDI
Model / Reference
S10ML FDA UDI
Description
Reli® Syringe, 10ML, 100ea/bx, 15bx/cs FDA UDI

Identifiers

Catalog Number
S10ML FDA UDI
Primary DI / UDI-DI
00386120011806 FDA UDI
FDA Product Code
FMF FDA UDI
GMDN Term
General-purpose syringe/needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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 — 10 Milliliter FDA UDI

Category: General-purpose syringe/needle

Reli® by Myco Medical Supplies Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose syringe/needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 347a7ac9-2375-43f5-a147-d2aa41f9fa7a 35 fields · synced May 31, 2026