Identity
- Trade Name
- N/A (Approved Vendor) FDA UDI
- Generic Name
- Specimen transfer scooping tool IVD FDA UDI
- Device Name
- Pipette,4mL,PK500 FDA UDI
- Model / Reference
- 21F238 FDA UDI
- Description
- Pipette,4mL,PK500 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10194484321502 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
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Also classified as Specimen transfer scooping tool IVD.
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Grainger International, Inc.
Sources (1)
- FDA UDI 2bf704bb-d482-4996-8a75-efa88a72a6d0 33 fields · synced Jun 8, 2026