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Vacsure Safety Multi-Sample Needle Only , 22g X 1 1/4"
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- VACSURE SAFETY MULTI-SAMPLE NEEDLE ONLY , 22G X 1 1/4" FDA UDI
- Generic Name
- Hypodermic needle, single-use FDA UDI
- Device Name
- SAFETY MULTI-SAMPLE NEEDLE ONLY, 22G X 1 1/4", Each FDA UDI
- Model / Reference
- VM-1022 FDA UDI
- Description
- SAFETY MULTI-SAMPLE NEEDLE ONLY, 22G X 1 1/4", Each FDA UDI
Identifiers
- Catalog Number
- VM-1022 FDA UDI
- Primary DI / UDI-DI
- 00850014448011 FDA UDI
- FDA Product Code
- FMF FDA UDI
- GMDN Term
- Hypodermic needle, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5860 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Hypodermic needle, single-use
Vacsure Safety Multi-Sample Needle Only , 22g X 1 1/4" by Labotek Group Corp — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Labotek Group Corp
Sources (1)
- FDA UDI e4ab7c5e-fcc0-421d-b876-43ce1e03f8bb 36 fields · synced Jun 6, 2026