Identity
- Trade Name
- HyperLight Leg Section FDA UDI
- Generic Name
- Universal operating table top FDA UDI
- Device Name
- HyperLight Transfer Board FDA UDI
- Model / Reference
- 08-075-81 FDA UDI
- Description
- HyperLight Transfer Board FDA UDI
Identifiers
- Catalog Number
- 08-075-81 FDA UDI
- Primary DI / UDI-DI
- 04946329307689 FDA UDI
- FDA Product Code
- GDC FDA UDI
- GMDN Term
- Universal operating table top FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4960 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
Yes
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
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 820 Millimeter FDA UDI
Category: Universal operating table top
HyperLight Leg Section by Mizuho Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Universal operating table top.
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- Carbon fibre back plate — Maquet, Inc. · Class I
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
- Mizuho Corporation
Sources (1)
- FDA UDI 84bc98ab-0b6e-4e7f-9df6-c1b58556637a 36 fields · synced Jun 8, 2026