Identity
- Trade Name
- Unipack Sterilization Wrap FDA UDI
- Generic Name
- Sterilization packaging, single-use FDA UDI
- Device Name
- 20" x 20" - Sterilization Wrap for Steam / ETO / Gamma FDA UDI
- Model / Reference
- UPP-2020 FDA UDI
- Description
- 20" x 20" - Sterilization Wrap for Steam / ETO / Gamma FDA UDI
Identifiers
- Catalog Number
- UPP-2020 FDA UDI
- Primary DI / UDI-DI
- D784UPP20201 FDA UDI
- FDA Product Code
- KCT FDA UDI
- GMDN Term
- Sterilization packaging, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6850 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Unipack Sterilization Wrap by Unipack Medical 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
- Unipack Medical Corporation
Sources (1)
- FDA UDI 3ae4012d-4c45-49c2-958f-2a7385e21efc 36 fields · synced May 30, 2026