FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 10888277374591 · Model: 512HRR · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
MEDLINE
Primary DI
10888277374591
Version / Model
512HRR
Catalog Number
512HRR
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-01-29
Public Version
1
Public Version Date
2025-02-06
Public Version Status
New
Public Device Record Key
2dc3d2e2-1dbb-4082-9f75-e87bed41a80e

Device Description

512HR @ENDPH TROCAR DISP SLEEVE HOUSING,

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NLM Laparoscope, general & plastic surgery, reprocessed

GMDN Terms

Code Name
61813 Laparoscopic access cannula, reprocessed

Identifiers

Type ID
Package 20888277374598
Primary 10888277374591

Customer Contacts