Identity
- Trade Name
- Capillary Caps FDA UDI
- Generic Name
- Capillary blood collection tube IVD, electrolyte-balanced heparin FDA UDI
- Device Name
- 100 capillary caps. An in vitro diagnostics medical device for use with Siemens Healthcare Diagnostics Multicap® and Multicap-S 2.34mm OD blood collection capillary tubes. FDA UDI
- Model / Reference
- 10311054 FDA UDI
- Description
- 100 capillary caps. An in vitro diagnostics medical device for use with Siemens Healthcare Diagnostics Multicap® and Multicap-S 2.34mm OD blood collection capillary tubes. FDA UDI
Identifiers
- Catalog Number
- 478605 FDA UDI
- Primary DI / UDI-DI
- 00630414115801 FDA UDI
- FDA Product Code
- GIO FDA UDI
- GMDN Term
- Capillary blood collection tube IVD, electrolyte-balanced heparin FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.6150 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: Capillary blood collection tube IVD, electrolyte-balanced heparin
Capillary Caps by Siemens Healthcare Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Siemens Healthcare Diagnostics
Sources (1)
- FDA UDI a18b9f0e-80b7-4c23-8f9d-a32edaff92cc 35 fields · synced May 30, 2026