Identity
- Trade Name
- ReNew Mini Endocut Scissor EUDAMEDReNew FDA UDI
- Generic Name
- Flexible endoscopic scissors, reusable FDA UDI
- Device Name
- ReNew Reusable Tips EUDAMEDMini Endocut Scissor Tip, Reusable FDA UDI
- Model / Reference
- 3151 EUDAMEDFDA UDI
- Description
- Mini Endocut Scissor Tip, Reusable FDA UDI
Identifiers
- Catalog Number
- 3151 FDA UDI
- Primary DI / UDI-DI
- 00811099014010 EUDAMED00811099011897 FDA UDI
- Basic UDI-DI
- 081109901DOC005SD EUDAMED
- Direct Marketing DI
- 00811099014010 EUDAMED
- FDA Product Code
- GEI FDA UDI
- EMDN Code
- L1204 LAPAROSCOPIC AND THORACOSCOPIC SURGERY FORCEPS, REUSABLE EUDAMED
- GMDN Term
- Flexible endoscopic scissors, reusable FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 878.4400 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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 — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Flexible endoscopic scissors, reusable.
- Scissors — SOPRO-COMEG GmbH · Class II
- ELMED — ELMED INCORPORATED · Class I
- Vasoview VV6 Pro — Maquet Cardiovascular LLC · Class II
- Edoscopic Dissection Probe — Medtronic PS Medical · Class II
- 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 (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Microline Surgical, Inc.
Sources (2)
- FDA UDI 2ba9ba4a-5b39-4767-a738-5b748b81e2e4 34 fields · synced Jul 8, 2026
- EUDAMED b9f121ed-6233-4add-b13d-6e3e46de1d99 61 fields · synced Jul 8, 2026