FDA UDI In Commercial Distribution 🇺🇸 United States

MaxMoreSpine

DI: 04260200310040 · Model: 1001-ABR 4 · 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
04260200310040
Version / Model
1001-ABR 4
Company Name
Hoogland Spine Products GmbH
Labeler DUNS
507292204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-28
Public Version
1
Public Version Date
2022-03-08
Public Version Status
New
Public Device Record Key
24e31d92-c91d-4920-a709-c773100600f3

Device Description

Abrasions device spoon tip, bent

Device Characteristics

Single Use
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
FZS Curette, Surgical, General Use

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary 04260200310040