Identity
- Trade Name
- RD® QUICK LOAD® FDA UDI
- Generic Name
- Polyolefin/fluoropolymer suture, monofilament FDA UDI
- Device Name
- RD® QUICK LOAD® SURGICAL SUTURE, 2-0 POLYPROPYLENE, NON-ABSORBABLE, 53", BLUE, MONOFILAMENT FDA UDI
- Model / Reference
- 020989 FDA UDI
- Description
- RD® QUICK LOAD® SURGICAL SUTURE, 2-0 POLYPROPYLENE, NON-ABSORBABLE, 53", BLUE, MONOFILAMENT FDA UDI
Identifiers
- Catalog Number
- 020989 FDA UDI
- Primary DI / UDI-DI
- 00850200006315 FDA UDI
- FDA Product Code
- GAW FDA UDI
- GMDN Term
- Polyolefin/fluoropolymer suture, monofilament FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.5010 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 53 Inch FDA UDI
Category: Polyolefin/fluoropolymer suture, monofilament
Rd® Quick Load® by LSI Solutions, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Polyolefin/fluoropolymer suture, monofilament.
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Cleared under the same submission
K031443 also covers:
K100593 also covers:
- C1® DEPTH LIMITER — LSI Solutions, Inc.
- C1® DEVICE — LSI Solutions, Inc.
- C1® DEVICE — LSI Solutions, Inc.
- COR-KNOT MINI® — LSI Solutions, Inc.
- COR-KNOT MINI® — LSI Solutions, Inc.
- COR-KNOT® — LSI Solutions, Inc.
- COR-KNOT® — LSI Solutions, Inc.
- COR-KNOT® QUICK LOAD® — LSI Solutions, Inc.
- COR-KNOT® QUICK LOAD® — LSI Solutions, Inc.
- COR-SUTURE® QUICK LOAD® — LSI Solutions, Inc.
- COR-SUTURE® QUICK LOAD® — LSI Solutions, Inc.
- COR-SUTURE® QUICK LOAD® — LSI Solutions, Inc.
K203120 also covers:
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
- LSI Solutions, Inc.
Sources (1)
- FDA UDI 337d82c6-0272-4808-a5cb-49f180100098 37 fields · synced May 30, 2026