Identity
- Trade Name
- ReNew FDA UDI
- Generic Name
- Flexible endoscopic scissors, reusable FDA UDI
- Device Name
- ReNew Laparoscopic Microscissor Scissors Tip, Reusable FDA UDI
- Model / Reference
- 3121 FDA UDI
- Description
- ReNew Laparoscopic Microscissor Scissors Tip, Reusable FDA UDI
Identifiers
- Catalog Number
- 3121 FDA UDI
- Primary DI / UDI-DI
- 00811099011873 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Flexible endoscopic scissors, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Flexible endoscopic scissors, reusable
ReNew by Microline Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Flexible endoscopic scissors, reusable.
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- ELMED — ELMED INCORPORATED · Class I
- Gyrus ACMI — Gyrus Acmi, Inc. · Class I
- ELMED — ELMED INCORPORATED · Class I
- HYSAFE — Richard Wolf GmbH · 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
- Microline Surgical, Inc.
Sources (1)
- FDA UDI 8675562c-fd34-4fbd-bea9-6fd0ecb0c0cc 34 fields · synced Jun 1, 2026