Identity
- Trade Name
- McKesson FDA UDI
- Generic Name
- Surgical eye pressure shield FDA UDI
- Device Name
- Eye protector Sterile Double Foam Adult FDA UDI
- Model / Reference
- 159-23 FDA UDI
- Description
- Eye protector Sterile Double Foam Adult FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10612479210162 FDA UDI
- FDA Product Code
- HOY FDA UDI
- GMDN Term
- Surgical eye pressure shield FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4750 FDA UDI
- 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
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Surgical eye pressure shield
McKesson by Mckesson Medical-Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Surgical Eye Shield — JARDON EYE PROSTHETICS, 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
- Mckesson Medical-Surgical Inc.
Sources (1)
- FDA UDI 2911b56e-32b4-4a54-99c5-27d5eb5ce92a 33 fields · synced Jun 8, 2026