← Back to catalogue

Inoculating Needle Rigid perforated bag packTypenex LP0302PF

FDA UDI

Class I (US FDA UDI)

by Zhejiang Runlab Technology Co., Ltd

Identity

Trade Name
Inoculating Needle Rigid perforated bag packTypenex LP0302PF FDA UDI
Generic Name
Specimen transfer scooping tool IVD FDA UDI
Device Name
Inoculating Needle Rigid perforated bag packTypenex LP0302PF FDA UDI
Model / Reference
Rigid, Dark blue, LP0302PF FDA UDI
Description
Inoculating Needle Rigid perforated bag packTypenex LP0302PF FDA UDI

Identifiers

Catalog Number
LP0302PF FDA UDI
Primary DI / UDI-DI
06973267013240 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 Needle Rigid perforated bag packTypenex LP0302PF by Zhejiang Runlab Technology Co., Ltd — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Specimen transfer scooping tool IVD.

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

Manufacturer
Zhejiang Runlab Technology Co., Ltd

Sources (1)

  • FDA UDI c0a0c423-ee64-462b-953a-6c078577060c 34 fields · synced Jun 1, 2026