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Inoculation Loops

FDA UDI

Class I (US FDA UDI)

by Copan Italia Spa

Identity

Trade Name
Inoculation Loops FDA UDI
Generic Name
Inoculating tool IVD, manual FDA UDI
Device Name
STERILE HARD 1 µL LOOPS IN RESEALABLE BAG OF 40 PCS FDA UDI
Model / Reference
8175CSR40H FDA UDI
Description
STERILE HARD 1 µL LOOPS IN RESEALABLE BAG OF 40 PCS FDA UDI

Identifiers

Catalog Number
8175CSR40H FDA UDI
Primary DI / UDI-DI
28053326004265 FDA UDI
FDA Product Code
LXG FDA UDI
GMDN Term
Inoculating tool IVD, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Inoculating tool IVD, manual

Inoculation Loops by Copan Italia Spa — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Inoculating tool IVD, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Copan Italia Spa

Sources (1)

  • FDA UDI 4537cb8e-7d87-4b19-ac1c-c8f88d2d3ea3 34 fields · synced Jun 8, 2026