Identity
- Trade Name
- CARBO FDA UDI
- Generic Name
- Acupuncture needle, single-use FDA UDI
- Device Name
- Classic Series CT1 Blister Pack with tube FDA UDI
- Model / Reference
- CT1-3620 FDA UDI
- Description
- Classic Series CT1 Blister Pack with tube FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06931833108875 FDA UDI
- FDA Product Code
- MQX FDA UDI
- GMDN Term
- Acupuncture needle, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5580 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
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
Yes
FDA UDI
Category: Acupuncture needle, single-use
A comprehensive device overview, including its features, compliance status, and FAQs. This device is used for stimulating peripheral nerves to produce surgical anaesthesia, relieve pain, and promote therapeutic effects.
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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
- WuJiang City Cloud&Dragon Medical Device Co., Ltd.
Sources (1)
- FDA UDI 741f2d99-6552-45a3-abbb-d00b081cdedd 33 fields · synced Oct 6, 2026