FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10886705016006 · Model: 281338 · DEPUY MITEK, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886705016006
Version / Model
281338
Catalog Number
281338
Company Name
DEPUY MITEK, LLC
Labeler DUNS
190572854
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-01
Public Version
4
Public Version Date
2021-01-28
Public Version Status
Update
Public Device Record Key
c929a777-e596-4819-a09d-aedb221530ca
Distribution End Date
2021-01-28

Device Description

Obturator for Storz / Linvatec sheath (281332)

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
Yes
Has Lot/Batch Number
No
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
HNX DEPRESSOR, ORBITAL

GMDN Terms

Code Name
35692 Rigid endoscope obturator

Identifiers

Type ID
Primary 10886705016006

Customer Contacts