Instrument, Clip Removal
Neurology · 21 CFR 882.4200
Recent MDR events
7 adverse event reports on file
- LAPRO-CLIPFeb 14, 2022MalfunctionCovidien Lp Llc North Haven1219930-2022-00538
- LAPRO-CLIPJan 7, 2020MalfunctionCovidien Lp Llc North Haven1219930-2020-00221
- WECK HEM-O-LOCKMar 2, 2017InjuryTeleflexMW5068274
- WECK HEM-O-LOKDec 24, 2013MalfunctionTelefex Medical3588765
- HEMOLOK REMOVER XL/L ENDOMay 28, 2010MalfunctionTeleflex Medical1044475-2010-00058
- HEMOLOK REMOVER XL/LMay 27, 2010MalfunctionTeleflex Medical1044475-2010-00053
- HEMOLOK REMOVER XL/LApr 20, 2010MalfunctionTeleflex Medical1044475-2010-00048
Event type breakdown
Most-reported manufacturers
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
28 firms currently registered for this product code
Mian Shahid Corp.
MUZAFFAR PUR, SIALKOT Punjab, PK
Mikron Precision, Inc.
GARDENA, CA, US
Aesculap Ag
TUTTLINGEN, DONAU Baden-Wurttemberg, DE
Tonglu Wanhe Medical Instrument Co., Ltd.
Hangzhou Zhejiang, CN
Tecomet, Inc.
KENOSHA, WI, US
Aspen Surgical Products, Inc.
Caledonia, MI, US
Teleflex Medical Llc
Morrisville, NC, US
Huzhou Junda Industry Co., Ltd.
Anji Zhejiang, CN
Addn Solutions Gmbh & Co. Kg
Wurmlingen Baden-Wurttemberg, DE
Acra Cut, Inc.
ACTON, MA, US
Wexler Surgical, Inc.
HOUSTON, TX, US
Comfort Surgical Instruments
Sialkot Punjab, PK
Xinhua Surgical Instrument Co. Ltd.
ZIBO Shandong, CN
Industrias Apson S.a De C.v
AGUA PRIETA Sonora, MX
Falcon Surgical Co. (pvt.) Ltd.
Sialkot Punjab, PK
Aesculap, Inc.
CENTER VALLEY, PA, US
Crown Surgical Corp.
Sialkot Punjab, PK
Teleflex Llc (nadc)
Olive Branch, MS, US
Covidien
North Haven, CT, US
Unlimited Surgical
Long Beach, CA, US
Hangzhou Kangji Medical Instrument Co., Ltd.
HANGZHOU Zhejiang, CN
Fengh Medical Co., Ltd.
Jiangyin Jiangsu, CN
Qsa Surgical (pvt) Ltd.
SIALKOT Punjab, PK
Berger Surgical Medical Products Gmbh
Neuhausen ob Eck Baden-Wurttemberg, DE
Ultimate Medical Products Ltd.
SHARJAH Ash Shariqah, AE
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for this product code.