Identity
- Trade Name
- SUPER VIEW® Pack for ZEISS RESIGHT® FDA UDI
- Generic Name
- Medical equipment/instrument drape, single-use FDA UDI
- Device Name
- 1 Each 40226 ZEISS RESIGHT® Disposable Lens Set & 1 Each ZEISS RESIGHT® Full Body Drape. Distributed by THEA Surgical (Insight's REF 40225) FDA UDI
- Model / Reference
- TS-RP-7002 FDA UDI
- Description
- 1 Each 40226 ZEISS RESIGHT® Disposable Lens Set & 1 Each ZEISS RESIGHT® Full Body Drape. Distributed by THEA Surgical (Insight's REF 40225) FDA UDI
Identifiers
- Catalog Number
- 40225 FDA UDI
- Primary DI / UDI-DI
- 00856222004841 FDA UDI
- GMDN Term
- Medical equipment/instrument drape, single-use FDA UDI
Classification
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 13 Millimeter FDA UDIOuter Diameter — 18 Millimeter FDA UDI
Category: Medical equipment/instrument drape, single-useOphthalmic diagnostic condensing lensVitrectomy contact lens, single-use
SUPER VIEW® Pack for ZEISS RESIGHT® by Insight Instruments, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- PHAKOS — Phakos · Class II
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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Insight Instruments, Inc.
Sources (1)
- FDA UDI f5a8bbda-a91c-4980-9d9e-488cc725d8e2 36 fields · synced May 30, 2026