Identity
- Trade Name
- Alleset FDA UDI
- Generic Name
- Non-dedicated vascular surgical procedure kit FDA UDI
- Device Name
- Arterial Pack_Sterile_2EA/CS FDA UDI
- Model / Reference
- TUF019 FDA UDI
- Description
- Arterial Pack_Sterile_2EA/CS FDA UDI
Identifiers
- Primary DI / UDI-DI
- 16931918142616 FDA UDI
- FDA Product Code
- OEZ FDA UDI
- GMDN Term
- Non-dedicated vascular surgical procedure kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1200 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
No
FDA UDI
Category: Non-dedicated vascular surgical procedure kit
Alleset by GRI Medical & Electronic Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Non-dedicated vascular surgical procedure kit.
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
- GRI Medical & Electronic Technology Co., Ltd.
Sources (1)
- FDA UDI 76702cd6-32dc-45b9-9010-b063f6a076be 34 fields · synced Sep 18, 2026