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N/A (Approved Vendor)

FDA UDI

Class I (US FDA UDI)

by Grainger International, Inc.

Identity

Trade Name
N/A (Approved Vendor) FDA UDI
Generic Name
Specimen transfer scooping tool IVD FDA UDI
Device Name
Disposable Transfer Pipet,5mL,PK500 FDA UDI
Model / Reference
21F225 FDA UDI
Description
Disposable Transfer Pipet,5mL,PK500 FDA UDI

Identifiers

Primary DI / UDI-DI
10194484321434 FDA UDI
FDA Product Code
GJW FDA UDI
GMDN Term
Specimen transfer scooping tool IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.6160 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Specimen transfer scooping tool IVD

N/A (Approved Vendor) by Grainger International, Inc. — 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

Sources (1)

  • FDA UDI eddb3922-c0c6-4094-a63a-bd846af76515 33 fields · synced Jun 8, 2026