← Back to catalogue

Reli®

FDA UDI

Class II (US FDA UDI)

by Myco Medical Supplies Inc.

Identity

Trade Name
RELI® FDA UDI
Generic Name
Spinal needle, single-use FDA UDI
Device Name
Introducer Needle 20G x 30mm, Sterile, 25/BX, 4BX/CS FDA UDI
Model / Reference
INT201251 FDA UDI
Description
Introducer Needle 20G x 30mm, Sterile, 25/BX, 4BX/CS FDA UDI

Identifiers

Catalog Number
INT201251 FDA UDI
Primary DI / UDI-DI
00386120010793 FDA UDI
FDA Product Code
BSP FDA UDI
GMDN Term
Spinal needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5150 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
Length — 30 Millimeter FDA UDI
Needle Gauge — 20 Gauge FDA UDI

Category: Spinal 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 Spinal needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI f585f49b-de43-4020-b5e2-04ca563ba5b8 35 fields · synced May 31, 2026