FDA UDI In Commercial Distribution 🇺🇸 United States

DORO COBRA® Retractor System

DI: 04250435527009 · Model: 1201.020 · pro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DORO COBRA® Retractor System
Primary DI
04250435527009
Version / Model
1201.020
Company Name
pro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung
Labeler DUNS
313517922
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-15
Public Version
6
Public Version Date
2021-05-10
Public Version Status
Update
Public Device Record Key
e4bda0af-ee66-4d94-afd2-637e8dccf8c5

Device Description

DORO COBRA® Retractor System consists of: 1201.021 1201.007 3116-111 3116-121 3116-131 3116-141 3116-151 1201.091

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HBL Holder, Head, Neurosurgical (Skull Clamp)

GMDN Terms

Code Name
46774 Surgical retractor/retraction system blade, reusable
45181 Surgical retraction system, reusable

Identifiers

Type ID
Primary 04250435527009

Premarket Submissions

Submission Number Supplement Number
K001808 000