Identity
- Trade Name
- IQLung (PR) FDA UDI
- Generic Name
- Blood collection set, invasive FDA UDI
- Device Name
- Sample Collection Kit FDA UDI
- Model / Reference
- 8 FDA UDI
- Description
- Sample Collection Kit FDA UDI
Identifiers
- Catalog Number
- 55 FDA UDI
- Primary DI / UDI-DI
- G29255080 FDA UDI
- GMDN Term
- Blood collection set, invasive FDA UDI
Classification
- 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
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
Category: Blood collection set, invasive
IQLung (PR) by Biodesix, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Blood collection set, invasive.
- MEDLINE — MEDLINE INDUSTRIES, INC. · Class II
- Custom Healthcare Systems Inc. — Manus Medical, LLC · Class II
- KBMED — KB Medical (group), Inc. · Class II
- MediChoice — OWENS & MINOR DISTRIBUTION, INC. · Class II
- SOL-CARE™ Safety Blood Collection Needle — Sol-Millennium Medical, Inc. · Class II
- SteriPath Gen2, 23G, BD — MAGNOLIA MEDICAL TECHNOLOGIES, INC. · Class II
- RELI® — MYCO MEDICAL SUPPLIES INC. · Class II
- Kawasumi — Jiangsu Caina Medical Co., Ltd · Class II
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 | N/A | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Biodesix, Inc.
Sources (1)
- FDA UDI 25d7178f-4207-46d5-ae4d-ec877e1170ba 34 fields · synced Jun 8, 2026