Identity
- Trade Name
- Alleset FDA UDI
- Generic Name
- Instrument management bag FDA UDI
- Device Name
- Diathermy Pouch_30x50cm_3-Pockets_w/ adhesive_Sterile_100ea/cs FDA UDI
- Model / Reference
- Model 80-14806-S FDA UDI
- Description
- Diathermy Pouch_30x50cm_3-Pockets_w/ adhesive_Sterile_100ea/cs FDA UDI
Identifiers
- Primary DI / UDI-DI
- 16931918115344 FDA UDI
- FDA Product Code
- PUI FDA UDI
- GMDN Term
- Instrument management bag FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4370 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
Ethylene Oxide FDA UDI
Category: Instrument management bag
Alleset by GRI Medical & Electronic Technology Co., Ltd. — 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
- GRI Medical & Electronic Technology Co., Ltd.
Sources (1)
- FDA UDI 2c9f0b64-9c55-498e-b1a4-c88cdc376d27 34 fields · synced Sep 18, 2026