Identity
- Trade Name
- OmniSight™ FDA UDI
- Generic Name
- Touchscreen FDA UDI
- Model / Reference
- OMST1065 FDA UDI
Identifiers
- Catalog Number
- OMST1065 FDA UDI
- Primary DI / UDI-DI
- 00889024596078 FDA UDI
- FDA Product Code
- OUG FDA UDI
- GMDN Term
- Touchscreen FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6310 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Width — 65.00 Inch FDA UDI
Category: Touchscreen
OmniSight™ by Zimmer Orthopaedic Surgical Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Touchscreen.
- VP2000 — Abbott Molecular · Class I
- OmniSight™ — Zimmer Orthopaedic Surgical Products · 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
- Zimmer Orthopaedic Surgical Products
Sources (1)
- FDA UDI 41b4aa1e-ec81-4b5b-97cb-957ffde282d2 35 fields · synced Jun 1, 2026