← Back to catalogue

HWATO Vaccaria seed W/P-50, with Tape

FDA UDI

Class I (US FDA UDI)

by Suzhou Medical Appliance Factory

Identity

Trade Name
HWATO Vaccaria seed W/P-50, with Tape FDA UDI
Generic Name
Ear microsystem seed/pellet FDA UDI
Device Name
50 Units in single pack FDA UDI
Model / Reference
W/P-50 (50 PCS) FDA UDI
Description
50 Units in single pack FDA UDI

Identifiers

Primary DI / UDI-DI
16901452983860 FDA UDI
FDA Product Code
KNM FDA UDI
GMDN Term
Ear microsystem seed/pellet FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5765 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ear microsystem seed/pellet

HWATO Vaccaria seed W/P-50, with Tape by Suzhou Medical Appliance Factory — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ear microsystem seed/pellet.

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 9c548cc0-5785-4338-b8f7-0b917ccf83fb 33 fields · synced May 30, 2026