Identity
- Trade Name
- CSH CANNULA FDA UDI
- Generic Name
- Tissue injection cannula FDA UDI
- Device Name
- CANNULA FDA UDI
- Model / Reference
- CSH-30019 FDA UDI
- Description
- CANNULA FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04580708063072 FDA UDI
- FDA Product Code
- GEA FDA UDI
- GMDN Term
- Tissue injection cannula FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Yes
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
Dimensions & Sizes
- Size
- Length — 19 Millimeter FDA UDIOuter Diameter — 0.3 Millimeter FDA UDI
Category: Tissue injection cannula
Csh Cannula by Tsk Laboratory, Japan — 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
- Tsk Laboratory, Japan
Sources (1)
- FDA UDI 1b0b8037-bb37-4fdd-9403-ef6a2329f93a 34 fields · synced May 30, 2026