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Tempo

FDA UDI

Class II (US FDA UDI)

by Blue Poppy Enterprises

Identity

Trade Name
Tempo FDA UDI
Generic Name
Acupuncture needle, single-use FDA UDI
Device Name
Tempo J-Type 2550 FDA UDI
Model / Reference
2550 FDA UDI
Description
Tempo J-Type 2550 FDA UDI

Identifiers

Primary DI / UDI-DI
10854166000162 FDA UDI
510(k) Number
K150903 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Acupuncture needle, single-use

Tempo by Blue Poppy Enterprises — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Acupuncture needle, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1cf09a3b-c0cf-4398-8ced-4d8b3ee2469a 34 fields · synced May 30, 2026