FDA Registration Active 🇨🇳 China

BEILUN PLASTECH INC

Reg #: 3009889060 · FEI: 3009889060 · Expires 2026
Products
13
Proprietary Names
0
Establishment Types
1
Classifications
13

Registration Details

Registration Name
BEILUN PLASTECH INC
Registration Number
3009889060
FEI Number
3009889060
Status
Active
Expiry Year
2026
Initial Importer
No
Address
No 18, Moju Rd, Daqi Industry Zone
City
Ningbo Zhejiang
Country
CN

Owner / Operator

Firm Name
Beilun Plastech Inc
Operator Number
10041867
Address
No 18, Moju Rd, Daqi Industry Zone
City
Ningbo
State
Zhejiang
Postal Code
315806
Country
CN

Products

Device Name Product Code
Kit, Surgical Instrument, Disposable KDD
Tubes, Vials, Systems, Serum Separators, Blood Collection JKA
Instrument, Ligature Passing And Knot Tying HCF
Catheter, Cholangiography GBZ
Guide, Surgical, Instrument FZX
Apparatus, Suction, Single Patient Use, Portable, Nonpowered GCY
Massager, Therapeutic, Electric ISA
Laparoscope, General & Plastic Surgery GCJ
Endoscopic Cholangiogram Kit NWT
Instrument, Surgical, Disposable KDC
Applicator, Ent KCJ
Dissector, Surgical, General & Plastic Surgery GDI
Blade, Scalpel GES

Establishment Types

Manufacture Medical Device for Another Party (Contract Manufacturer)