Identity
- Trade Name
- CARDINAL HEALTH FDA UDI
- Generic Name
- Metered-delivery hypodermic syringe/needle FDA UDI
- Device Name
- EYE PACK FDA UDI
- Model / Reference
- SEYDHEPFAB FDA UDI
- Description
- EYE PACK FDA UDI
Identifiers
- Catalog Number
- SEYDHEPFAB FDA UDI
- Primary DI / UDI-DI
- 10197106210345 FDA UDI
- FDA Product Code
- OJK FDA UDI
- GMDN Term
- Metered-delivery hypodermic syringe/needle FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.4790 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
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
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: Metered-delivery hypodermic syringe/needle
Cardinal Health by Cardinal Health 200, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Metered-delivery hypodermic syringe/needle.
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- VanishPoint® — Retractable Technologies, Inc. · Class II
- Securegard — SafeGard Medical /Hungary/ Gyogyaszati Eszkozgyarto es Forgalmazo Korlatolt Felelossegu Tarsasag · Class II
- Safety Syringe w/Needle — Dynarex Corp. · Class II
- Magellan — Cardinalhealth · 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 | Class II | Pending data |
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Manufacturer
- Manufacturer
- Cardinal Health 200, LLC
Sources (1)
- FDA UDI e9eadf7e-5627-47b5-aa35-87162c6cbe34 34 fields · synced Jun 8, 2026