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Blue Diamond

FDA UDI

Class II (US FDA UDI)

by North Coast Medical, Inc.

Identity

Trade Name
Blue Diamond FDA UDI
Generic Name
Acupuncture needle, single-use FDA UDI
Device Name
Blue Diamond Dry Needle .30x50mm (100) FDA UDI
Model / Reference
NCBD-3050 FDA UDI
Description
Blue Diamond Dry Needle .30x50mm (100) FDA UDI

Identifiers

Catalog Number
4308 FDA UDI
Primary DI / UDI-DI
00768627160384 FDA UDI
FDA Product Code
MQX FDA UDI
GMDN Term
Acupuncture needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5580 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

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 0.30 Millimeter FDA UDI
Shaft Length — 50 Millimeter FDA UDI

Category: Acupuncture needle, single-use

Blue Diamond by North Coast Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Acupuncture needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7608e0d6-5eb6-4b9b-8f1a-62bc579280ef 36 fields · synced May 31, 2026