Identity
- Trade Name
- Oasis FDA UDI
- Generic Name
- Patient surgical drape, single-use FDA UDI
- Device Name
- Sterile Surgical Drapes 60"X80" FDA UDI
- Model / Reference
- DR6080 FDA UDI
- Description
- Sterile Surgical Drapes 60"X80" FDA UDI
Identifiers
- Primary DI / UDI-DI
- B031DR60800 FDA UDI
- FDA Product Code
- KKX FDA UDIPUI 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
- Not 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Oasis by American Health Service Sales Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- American Health Service Sales Corporation
Sources (1)
- FDA UDI 0e2391b7-1f92-479f-af5f-a869946bde6f 34 fields · synced May 30, 2026