FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 07613154109760 · Model: 3910-003-020 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
NA
Primary DI
07613154109760
Version / Model
3910-003-020
Catalog Number
3910-003-020
Company Name
STRYKER CORPORATION
Labeler DUNS
187502109
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-04
Public Version
4
Public Version Date
2022-12-12
Public Version Status
Update
Public Device Record Key
921a960a-90da-4934-b653-343e2906081e
Distribution End Date
2022-12-11

Device Description

OBTURATOR

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
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
NBH ACCESSORIES,ARTHROSCOPIC

GMDN Terms

Code Name
33997 Surgical drill guide obturator

Identifiers

Type ID
Primary 07613154109760

Customer Contacts