Identity
- Trade Name
- RACK+WT,5505(2),5581,5531,5539 (6 PC) FDA UDI
- Generic Name
- General-purpose casework FDA UDI
- Model / Reference
- 5566-100 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840314806345 FDA UDI
- FDA Product Code
- IOD FDA UDI
- GMDN Term
- General-purpose casework FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5350 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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: General-purpose casework
Rack+wt, 5505(2), 5581, 5531, 5539 (6 Pc) by Hausmann Enterprises, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as General-purpose casework.
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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 I | Pending data |
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Manufacturer
- Manufacturer
- Hausmann Enterprises, Llc
Sources (1)
- FDA UDI bff3d40c-4cae-4504-8128-aa0d749b19d9 32 fields · synced Jun 1, 2026