Identity
- Trade Name
- Invenio FDA UDI
- Generic Name
- Patient surgical drape, single-use FDA UDI
- Device Name
- Femoral Radial Angiography Drape _Extra Wide _169inx95.25in_Non-Sterile_12ea/cs FDA UDI
- Model / Reference
- i80-01220G FDA UDI
- Description
- Femoral Radial Angiography Drape _Extra Wide _169inx95.25in_Non-Sterile_12ea/cs FDA UDI
Identifiers
- Primary DI / UDI-DI
- 16931918134550 FDA UDI
- FDA Product Code
- PUI FDA UDI
- GMDN Term
- Patient surgical drape, single-use 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
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Patient surgical drape, single-use
Invenio 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 0943d4d4-0860-4e02-9acc-51c0cae1befc 34 fields · synced Sep 18, 2026