← Back to catalogue

Reli

FDA UDI

Class II (US FDA UDI)

by Myco Medical Supplies Inc.

Identity

Trade Name
RELI FDA UDI
Generic Name
Non-fixed blood collection needle FDA UDI
Device Name
RELI® Blood Collection Needle 21G x 1”, Sterile FDA UDI
Model / Reference
BCN-R21G101 FDA UDI
Description
RELI® Blood Collection Needle 21G x 1”, Sterile FDA UDI

Identifiers

Catalog Number
BCN-R21G101 FDA UDI
Primary DI / UDI-DI
10386120007981 FDA UDI
510(k) Number
K090426 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Non-fixed blood collection needle 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

Dimensions & Sizes

Size
Length — 1 Inch FDA UDI
Needle Gauge — 21 Gauge FDA UDI

Category: Non-fixed blood collection needle

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

Similar devices

Also classified as Non-fixed blood collection needle.

Cleared under the same submission

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 039a037e-2f8f-46f9-b69f-50bc26438435 36 fields · synced Jun 1, 2026