FDA Registration Active 🇩🇪 Germany

HERMANN MUELLER Medizintechnik GmbH

Reg #: 9680735 · FEI: 3004095748 · Expires 2026
Products
33
Proprietary Names
4
Establishment Types
4
Classifications
33

Registration Details

Registration Name
HERMANN MUELLER Medizintechnik GmbH
Registration Number
9680735
FEI Number
3004095748
Status
Active
Expiry Year
2026
Initial Importer
No
Address
DR. KARL-STORZ-STR. 3
City
TUTTLINGEN Baden-Wurttemberg
Country
DE

Regulatory Submissions

510(k) Number
K120117

Owner / Operator

Firm Name
Hermann Mueller Medizintechnik GmbH
Operator Number
9010992
Address
DR. KARL-STORZ-STR. 3, --
City
TUTTLINGEN
State
Baden-Wurttemberg
Postal Code
78532
Country
DE

US Agent

Business Name
BSI BUSINESS SUPPORT INTERNATIONAL
Contact Name
Angelika Scherp
Address
1350 Avenue of the Americas, 2nd Floor
City
New York
State
NY
ZIP
10019
Country
US
Phone
212 3318358

Products

Device Name Product Code
Applier, Surgical, Clip GDO
Contractor, Surgical FZR
Carver, Wax, Dental EIK
Curette, Surgical, General Use FZS
Speculum, Ent EPY
Chisel, Surgical, Manual FZO
Sterilization Wrap Containers, Trays, Cassettes & Other Accessories KCT
Knife, Surgical EMF
Retractor GAD
Gag, Mouth KBN
Rasp, Surgical, General & Plastic Surgery GAC
Tamp HXG
Explorer, Operative EKB
Osteotome HWM
Chisel, Osteotome, Surgical EMM
Probe HXB
Guide, Surgical, Instrument FZX
Dissector, Tonsil KBM
Elevator, Surgical, Dental EMJ
Retractor, All Types EIG
Speculum, Vaginal, Metal HDF
Stripper, Surgical HRT
File HTP
File, Bone, Surgical EMI
Tape, Measuring, Rulers And Calipers FTY
Retractor, Self-Retaining FFO
Instrument, Filling, Plastic, Dental EIY
Hook, Surgical, General & Plastic Surgery GDG
Elevator, Surgical, General & Plastic Surgery GEG
Scalpel, One-Piece GDX
Plugger, Root Canal, Endodontic EKR
Excavator, Dental, Operative EKC
Orthopedic Manual Surgical Instrument LXH

Proprietary Names

PROBE K2-588 VARIOUS TYPES OF DEN VARIOUS TYPES OF ORTHO

Establishment Types

Manufacture Medical Device for Another Party (Contract Manufacturer) Manufacture Medical Device Export Device to the United States But Perform No Other Operation on Device Repack or Relabel Medical Device