Identity
- Trade Name
- MICROSAFE FDA UDI
- Generic Name
- Capillary blood collection tube IVD, lithium heparin FDA UDI
- Device Name
- MICROSAFE, 35 ul FDA UDI
- Model / Reference
- 1035-25-01 FDA UDI
- Description
- MICROSAFE, 35 ul FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860001024067 FDA UDI
- FDA Product Code
- GIO FDA UDI
- GMDN Term
- Capillary blood collection tube IVD, lithium 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Capillary blood collection tube IVD, lithium heparin
Microsafe by Drummond Scientific Company — 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
- Drummond Scientific Company
Sources (1)
- FDA UDI 8cf9201f-c659-4a3c-b77a-e2fefe2b1293 33 fields · synced May 30, 2026