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Capillary Blood Specimen Collection Supplemental Pack
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Capillary Blood Specimen Collection Supplemental Pack FDA UDI
- Generic Name
- Capillary blood collection set, professional FDA UDI
- Device Name
- Capillary blood collection kit, professional FDA UDI
- Model / Reference
- 6 FDA UDI
- Description
- Capillary blood collection kit, professional FDA UDI
Identifiers
- Catalog Number
- 59 FDA UDI
- Primary DI / UDI-DI
- G292590 FDA UDI
- FDA Product Code
- PQD FDA UDI
- GMDN Term
- Capillary blood collection set, professional FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1675 FDA UDI
- Commercial Distribution
- Not 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
Yes
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
Capillary Blood Specimen Collection Supplemental Pack by Biodesix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 II | Pending data |
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Manufacturer
- Manufacturer
- Biodesix, Inc.
Sources (1)
- FDA UDI 94f4e9f7-1fd2-4125-97ed-8dda8ccbe5c6 35 fields · synced Jun 1, 2026