Identity
- Trade Name
- ReNew FDA UDI
- Generic Name
- Endoscopic electrosurgical handpiece/electrode, monopolar, reusable FDA UDI
- Device Name
- Renew Handle Ring Inserts, medium, Reusable FDA UDI
- Model / Reference
- 3910 FDA UDI
- Description
- Renew Handle Ring Inserts, medium, Reusable FDA UDI
Identifiers
- Catalog Number
- 3910 FDA UDI
- Primary DI / UDI-DI
- 00811099010654 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Endoscopic electrosurgical handpiece/electrode, monopolar, 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: Endoscopic electrosurgical handpiece/electrode, monopolar, reusable
ReNew by Microline Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Endoscopic electrosurgical handpiece/electrode, monopolar, reusable.
- Mediflex Deluxe Laparoscopic Instruments — FLEXBAR MACHINE CORP. · Class II
- Bowel Grasper Inner Shaft — ORANGE SURGICAL INSTRUMENTS, LLC · Class II
- AESCULAP — AESCULAP, INC. · Class II
- Hermann Medizintechnik GmbH — Hermann Medizintechnik GmbH · Class II
- Silex — SILEX MEDICAL, LLC · Class II
- AESCULAP — AESCULAP, INC. · Class II
- Signature — SILEX MEDICAL, LLC · Class II
- Dorsey Grasper Inner Shaft — ORANGE SURGICAL INSTRUMENTS, LLC · 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
- Microline Surgical, Inc.
Sources (1)
- FDA UDI 5f62b4de-53b8-465f-811b-f6e03dc8753b 34 fields · synced Jun 8, 2026