Identity
- Trade Name
- CARDINAL HEALTH FDA UDI
- Generic Name
- Ophthalmic surgical procedure kit, non-medicated, single-use FDA UDI
- Device Name
- DCSM CATARACT PACK FDA UDI
- Model / Reference
- SEYHDCPF30 FDA UDI
- Description
- DCSM CATARACT PACK FDA UDI
Identifiers
- Catalog Number
- SEYHDCPF30 FDA UDI
- Primary DI / UDI-DI
- 10197106647578 FDA UDI
- FDA Product Code
- OJK FDA UDI
- GMDN Term
- Ophthalmic surgical procedure kit, non-medicated, single-use 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: Ophthalmic surgical procedure kit, non-medicated, single-use
Cardinal Health's DCSM CATARACT PACK is a single-use, sterilized device designed for the treatment of cataracts. This device features a proprietary material called "DCSM," which provides excellent optical clarity and vision correction.
Similar devices
Also classified as Ophthalmic surgical procedure kit, non-medicated, single-use.
- 3 POLI-SAFE 60X45 C/ ADESIVO — Linea Sterile S.p.A. · Class I
- CustomEyes® — Beaver-Visitec International, Inc. · Class I
- LAPAROSCOPIC SLEEVE RESECTION PACK — Johnson & Johnson Medical GmbH · Class III
- KIT GINECOLOGIA LAPAROSCOPIA — Linea Sterile S.p.A. · Class I
- SET 273 Ambulant — BATIST Medical Productions s.r.o. · Class III
- THORAX PROCEDURE PACK — Johnson & Johnson Medical GmbH · Class III
- Implantace portu — PAUL HARTMANN AG · Class III
- Aligned Medical Solutions — Aligned Medical Solutions · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Cardinal Health 200, LLC
Sources (1)
- FDA UDI 0a4202fa-7dd9-4c01-873e-585c1b71e3cf 35 fields · synced Jul 24, 2026