Identity
- Trade Name
- Clover Retractor Set FDA UDI
- Generic Name
- Self-retaining surgical retractor, reusable FDA UDI
- Device Name
- Clover Retractor Set Consists of the Following: 1 x 7332-66, 4 x 7332-68, 2 x 7332-71, 1 x 7332-72,, 1 x 7332-73D, 1 x 7332-74D, 1 x 7332-75D, 1 x 7332-76D, 1 x 7332-86D, 1 x 7332-89D, 1 x 7332-77D, 1 x 7332-78, 2 x 7332-79, 2 x 7332-81, 2 x 7332-82, 2 x 7332-84, 1 x 7332-91, 1 x 7332-93, 1 x 7332-97, 1 x 7332-98, 2 x 7225-54B, 1 x 7233-54, 1 x 7233-56, 2 x 7218-18, 1 x 7042-42I, 1 x 7233-62, 1 x 7233-64, 1 x 7233-66, 1 x 7338-05, 1 x 7230-60, 1 x 7230-62, 1 x 7233-83, 1 x 7233-87& 1 x 7233-69 FDA UDI
- Model / Reference
- 7332-65 FDA UDI
- Description
- Clover Retractor Set Consists of the Following: 1 x 7332-66, 4 x 7332-68, 2 x 7332-71, 1 x 7332-72,, 1 x 7332-73D, 1 x 7332-74D, 1 x 7332-75D, 1 x 7332-76D, 1 x 7332-86D, 1 x 7332-89D, 1 x 7332-77D, 1 x 7332-78, 2 x 7332-79, 2 x 7332-81, 2 x 7332-82, 2 x 7332-84, 1 x 7332-91, 1 x 7332-93, 1 x 7332-97, 1 x 7332-98, 2 x 7225-54B, 1 x 7233-54, 1 x 7233-56, 2 x 7218-18, 1 x 7042-42I, 1 x 7233-62, 1 x 7233-64, 1 x 7233-66, 1 x 7338-05, 1 x 7230-60, 1 x 7230-62, 1 x 7233-83, 1 x 7233-87& 1 x 7233-69 FDA UDI
Identifiers
- Catalog Number
- 7332-65 FDA UDI
- Primary DI / UDI-DI
- 10840199543691 FDA UDI
- FDA Product Code
- GAD FDA UDI
- GMDN Term
- Self-retaining surgical retractor, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Self-retaining surgical retractor, reusable
Clover Retractor Set by Koros USA, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Koros USA, Inc.
Sources (1)
- FDA UDI a6d42363-b16e-4874-896f-19f58b5011da 37 fields · synced May 31, 2026