FDA Registration Active 🇨🇳 China

POSEIDON NJ2561, TTP-PNI-1, NJ1751, NJ5090, NJ5200, NJ5360, NJ5370

Reg #: 3015516536 · FEI: 3015516536 · Expires 2025
Products
1
Proprietary Names
25
Establishment Types
10
Classifications
1

Registration Details

Registration Name
NICEFEEL MEDICAL DEVICE TECHNOLOGY CO.,LTD.
Registration Number
3015516536
FEI Number
3015516536
Status
Active
Expiry Year
2025
Initial Importer
No
Address
Bldg 30th, Rm.201, Longwangmiao Industrial Park, Baishixia East Community, Fuyong Town, Bao'an District
City
SHENZHEN Guangdong
Country
CN

Owner / Operator

Firm Name
NICEFEEL MEDICAL DEVICE TECHNOLOGY CO.,LTD.
Operator Number
10060942
Address
Bldg 30th, Rm.201, Longwangmiao Industrial Park, Baishixia, East Community, Fuyong Town, Bao'an District
City
Shenzhen
State
Guangdong
Postal Code
518103
Country
CN
Correspondent
Tony Wan

US Agent

Business Name
ANTEK SERVICE INC.
Contact Name
Shirley Guo
Address
901 N PENNSYLVANIA ST STE 0
City
DENVER
State
CO
ZIP
80203
Country
US
Phone
303 8006306

Products

Device Name Product Code
Irrigator, Powered Nasal KMA

Proprietary Names

POSEIDON NJ2561, TTP-PNI-1, NJ1751, NJ5090, NJ5200, NJ5360, NJ5370 Nicefeel NJ1596, NJ3940, NJ5090, NJ1561, NJ256, NJ2630, NJ2581, NJ3832, NJ3921, NJ3950, NJ5091, NJ5240, NJ5260; Nicefeel NJ5060, NJ5070, NJ3841, NJ169, NJ5260, NJ5240; Nicefeel NJ5240, NJ5260; Nicefeel,NJ2920,NJ2910,NJ2540,NJ2900,NJ2650; NJ158,NJ162,NJ163,FC162,FC163,WF-600B,HP083A,EE-88,ARBD-901,EVD-010,IR-700,NJ169,FC169,LV03,W06,VL-1515,ZSTM169,DF-10; TMBH027,DCIR2,AW-2110,RL210,V6,DET-FC1620; DET-FC2620,DET-FC3620,EHFC-WP981A,EHFC-WP982B,RXFC-WP983C BLS1800,PHKWF1591,TMBH026,TZ317,FC1594,CLS01,FC1595,C300,FJ-0628,FJ-0628T,FJ-0628B,WF-202,TF200,IR-1001 KC-01,ZSTM-159,ORA001,IR-200,PI00695,90002PI,90011PI,90012PI,RC-909,DF-0010,DG-CX10,RL200,DJ159,IR-200,BN4337; IK-PCA004,WB-N1801YL,MRPC-FC166; GL-555,NJ288,FC288,TF600,YCT1,IK-PCA005,CF888,RL500,HOC580,X809S,IR-2003,O2 Water Flosser: WF-606; NJ2520,FC2521,NJ3610,NJ3620,NJ3630,NJ3640,NJ3650,NJ3660,NJ3670,NJ3680,NJ3690, Winner NJ159 Product Name: Nasal Rinse Mix. Model: B1(1.8g), B2(2.7g), B3(3.6g), B4(4.5g), B5, B6, B7, B8, B9; FC1521,EP23997,ZLL1831,PWF93,X6,FC1522,NJ2550,NJ2510; FC2550,NJ2550,NJ2510,FC2551,NJ2580,NJ2581,NJ2582FC2581,NJ2620,NJ2621 Nicefeel NJ175, NJ1521, NJ159, NJ165, NJ166, NJ168, NJ2650, NJ2660, NJ188, NJ288, NJ5060, NJ5070, NJ3841, NJ169, NJ1581; G188,BLS-2800,FC188-PK,FC188-WH,GB1900,F76-0004; HP045A,WF-9,BC-2009,TC530,FC169B,NJ168,FC168,HOC200,HC037,GB1700,UH-WF200,F76-0002 VL-1506,BLS-1600,G168,GL-777; J709,J711,SMC-TC1,IGACOOL,MS1914,HP114P,V6,WF-300H,PD300,EWF-32,V300,HP114A,NJ259,NJ2591,AL213; Nicefeel NJ159, NJ2660, NJ5060, NJ5070, NJ1521, NJ2650, NJ165, NJ188, NJ1581, NJ3841; Medisana NJ5260, NI 200, NJ5240, NI 250 SinuFlux SF-17601, NJ175; SinuPulse Traveler SPT300, NJ2660; NJ159,NJ1591,NJ1592,NJ1593,NJ1594,NJ1595,FC159X,FC1591,FC1952,FC1593,FC159,LV04,DQ14,BC-2007,OW02,DF-20,VL1513; ZHF166,DG-FC1591; CS520,RON1591,WF-300B,MD20,ZHF188,J708,J710,NJ156,P-121,IR-1002,DJ156,MF156 Nicefeel NJ5060, NJ5070, NJ159, NJ2660, NJ1581, NJ3841, NJ2650, NJ1521, NJ165, NJ188, NJ2561, NJ5240, NJ5260 Product Name: Nasal Rinse Mix. Model: A1(1.8g), A2(2.7g), A3(3.6g), A4(4.5g), A5, A6, A7, A8, A9; AJ-PCA033,IK-PCA016,CM-PCA005,NJ2610,NJ2660; GESS-707,IR-Z12,SWIE10002,WF-600B,D600,AW-2200,FC165B,NJ166,FC166,MF166,DJ166 GuruNanda NJ5240, 4000 NJ2661,NJ2660,NJ266,NJ2700,FC2720,NJ2730,NJ3810,NJ3820,NJ3830,NJ3840,NJ3850,NJ3860,NJ3870,NJ3880,NJ3890; NJ256,NJ2561,NJ2562,AW-2100,WB-N1802YL,FC2561,AJ-PCA028,ZHF186; DF1001,IR-1003,JF259,HACH-808,X628,NJ152,NJ1521,NJ1522,ZHF168

Establishment Types

Export Device to the United States But Perform No Other Operation on Device Repack or Relabel Medical Device Sterilize Medical Device for Another Party (Contract Sterilizer) Develop Specifications But Do Not Manufacture At This Facility Remanufacture Medical Device Manufacture Medical Device Manufacture Medical Device for Another Party (Contract Manufacturer) Foreign Private Label Distributor Complaint File Establishment per 21 CFR 820.198 Reprocess Single-Use Device