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Hareta

FDA UDI

Class I (US FDA UDI)

by Yancheng Jingwei Chemicals Co., Ltd

Identity

Trade Name
HARETA FDA UDI
Generic Name
Plasma filtration/collection kit IVD FDA UDI
Device Name
TRANSFER PIPETTE 3ML STERILE 500PCS/BOX AND 2000PCS/CASE FDA UDI
Model / Reference
PTRP003L-STR FDA UDI
Description
TRANSFER PIPETTE 3ML STERILE 500PCS/BOX AND 2000PCS/CASE FDA UDI

Identifiers

Primary DI / UDI-DI
06975800988664 FDA UDI
FDA Product Code
LGX FDA UDI
GMDN Term
Plasma filtration/collection kit IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Plasma filtration/collection kit IVD

Hareta by Yancheng Jingwei Chemicals Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Plasma filtration/collection kit IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Yancheng Jingwei Chemicals Co., Ltd

Sources (1)

  • FDA UDI 46c8cd30-b238-4a1c-8253-6becefc118d3 33 fields · synced May 30, 2026