Identity
- Trade Name
- Extraction cannula, LC FDA UDI
- Generic Name
- Collection syringe adaptor, single-use FDA UDI
- Device Name
- Extraction cannula, LC, Single-use FDA UDI
- Model / Reference
- Single-use LC Cannula FDA UDI
- Description
- Extraction cannula, LC, Single-use FDA UDI
Identifiers
- Catalog Number
- 655010-5 FDA UDI
- Primary DI / UDI-DI
- 04260170881427 FDA UDI
- FDA Product Code
- QKL FDA UDI
- GMDN Term
- Collection syringe adaptor, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.5040 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Collection syringe adaptor, single-use
Extraction cannula, LC by Human Med AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Extraction cannula — Human Med AG · Class II
- Extraction tube — Human Med AG · Class II
- Extraction cannula — Human Med AG · 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 | Class II | Pending data |
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Manufacturer
- Manufacturer
- Human Med AG
Sources (1)
- FDA UDI c9d11088-147d-4239-b09c-ae4b24235987 35 fields · synced May 31, 2026