FDA UDI In Commercial Distribution 🇺🇸 United States

MaxMoreSpine

DI: 04260200313102 · Model: 1001-BE-002 · Hoogland Spine Products GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
MaxMoreSpine
Primary DI
04260200313102
Version / Model
1001-BE-002
Company Name
Hoogland Spine Products GmbH
Labeler DUNS
507292204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-02
Public Version
1
Public Version Date
2022-08-10
Public Version Status
New
Public Device Record Key
ebae5cd5-0343-4a23-928e-529255dec09d

Device Description

Bipolar coagulation electrode, flexible

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
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
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
61872 Endoscopic electrosurgical electrode, bipolar, single-use

Identifiers

Type ID
Primary 04260200313102