FDA UDI Not in Commercial Distribution 🇺🇸 United States

DORO® Blade

DI: 04250435532003 · Model: 3116-132 · Black Forest Medical GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
DORO® Blade
Primary DI
04250435532003
Version / Model
3116-132
Company Name
Black Forest Medical GmbH
Labeler DUNS
313517922
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-30
Public Version
9
Public Version Date
2026-02-02
Public Version Status
Update
Public Device Record Key
3171d52c-6f86-4c67-8a61-99f95b42e1e1
Distribution End Date
2023-05-05

Device Description

DORO® Blade 152x16mm

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
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
HAO Instrument, Surgical, Non-Powered

GMDN Terms

Code Name
46774 Surgical retractor/retraction system blade, reusable

Identifiers

Type ID
Primary 04250435532003