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Inoculating Loop Typenex

FDA UDI

Class I (US FDA UDI)

by Zhejiang Runlab Technology Co., Ltd

Identity

Trade Name
Inoculating Loop Typenex FDA UDI
Generic Name
Specimen transfer scooping tool IVD FDA UDI
Device Name
10ul, Flexible, Blue FDA UDI
Model / Reference
10ul, Flexible, Blue FDA UDI
Description
10ul, Flexible, Blue FDA UDI

Identifiers

Catalog Number
LP0203 FDA UDI
Primary DI / UDI-DI
06973267012038 FDA UDI
FDA Product Code
LIB FDA UDI
GMDN Term
Specimen transfer scooping tool IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2660 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

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: Specimen transfer scooping tool IVD

Inoculating Loop Typenex by Zhejiang Runlab Technology Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Specimen transfer scooping tool IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zhejiang Runlab Technology Co., Ltd

Sources (1)

  • FDA UDI fcfd5157-317d-4b78-89b8-1a36f3649a7c 34 fields · synced May 30, 2026