FDA UDI In Commercial Distribution 🇺🇸 United States

Blade, 38mm

DI: 00810097800243 · Model: 1252-5520-238 · Osteocentric Technologies, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Blade, 38mm
Primary DI
00810097800243
Version / Model
1252-5520-238
Catalog Number
1252-5520-238
Company Name
Osteocentric Technologies, Inc.
Labeler DUNS
089645059
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-17
Public Version
5
Public Version Date
2025-01-08
Public Version Status
Update
Public Device Record Key
49bc844a-a0b0-421a-822e-43b7fd26314e

Device Description

Blade, 38mm

Device Characteristics

Single Use
Yes
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
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
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
GES Blade, Scalpel

GMDN Terms

Code Name
58849 Sacroiliac joint transarticular fixation/arthrodesis implantation kit

Identifiers

Type ID
Primary 00810097800243

Customer Contacts

Device Sizes

Type Value Unit Text
Length 38 Millimeter