Identity
- Trade Name
- NeoDevices, Inc. FDA UDI
- Generic Name
- Spinal needle, single-use FDA UDI
- Device Name
- Neonatal LP Needle 22ga x 1" FDA UDI
- Model / Reference
- LN2210 FDA UDI
- Description
- Neonatal LP Needle 22ga x 1" FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10816340021097 FDA UDI
- FDA Product Code
- FMI FDA UDI
- GMDN Term
- Spinal needle, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5570 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
No
FDA UDI
Category: Spinal needle, single-use
NeoDevices, Inc. by Neodevices Inc — 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
- Neodevices Inc
Sources (1)
- FDA UDI 83248ba2-0de1-41d2-8869-63f3809bbfd4 34 fields · synced May 30, 2026