Identity
- Trade Name
- Lite Touch FDA UDI
- Generic Name
- Hypodermic needle, single-use FDA UDI
- Device Name
- LiteTouch Safety Needle FDA UDI
- Model / Reference
- 600 FDA UDI
- Description
- LiteTouch Safety Needle FDA UDI
Identifiers
- Catalog Number
- 600 FDA UDI
- Primary DI / UDI-DI
- 00732671006004 FDA UDI
- FDA Product Code
- FMI FDA UDI
- GMDN Term
- Hypodermic 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
Yes
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Needle Gauge — 23 Gauge FDA UDILength — 1.0 Inch FDA UDI
Category: Hypodermic needle, single-use
Lite Touch by Amity Holdings, Llc — 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
- Amity Holdings, Llc
Sources (1)
- FDA UDI a2eec6ff-1bf3-48fd-9248-8f571fed45aa 37 fields · synced Jun 8, 2026