Identity
- Trade Name
- MEDI FDA UDI
- Generic Name
- Compression bandaging kit FDA UDI
- Device Name
- JUXTAFIT ESSENTIALS 28CM XL FDA UDI
- Model / Reference
- 70016000 FDA UDI
- Description
- JUXTAFIT ESSENTIALS 28CM XL FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00091037458803 FDA UDI
- FDA Product Code
- MDR FDA UDI
- GMDN Term
- Compression bandaging kit FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5160 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
Yes
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
Yes
FDA UDI
Medi by Medi Manufacturing, Inc. — Class I — 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medi Manufacturing, Inc.
Sources (1)
- FDA UDI 66e6eef1-b7c4-4504-b6e2-9814542b8adb 35 fields · synced May 31, 2026