← Back to catalogue

Eacu, Eaku, Zagu, Jocu

FDA UDI

Class II (US FDA UDI)

by Maanshan Bond Medical Instruments Co., Ltd.

Identity

Trade Name
EACU, EAKU, ZAGU, JOCU FDA UDI
Generic Name
Acupuncture needle, single-use FDA UDI
Model / Reference
CB5040 FDA UDI

Identifiers

Primary DI / UDI-DI
B338CB50401 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Acupuncture needle, single-use

Eacu, Eaku, Zagu, Jocu by Maanshan Bond Medical Instruments Co., Ltd. — 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

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

Manufacturer

Sources (1)

  • FDA UDI d7c315cb-2b6c-4f78-8c06-0fd07da770c1 33 fields · synced May 31, 2026