FDA UDI In Commercial Distribution 🇺🇸 United States

Medline Industries, Inc.

DI: 10889942352012 · Model: DYND04195 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Medline Industries, Inc.
Primary DI
10889942352012
Version / Model
DYND04195
Catalog Number
DYND04195
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-29
Public Version
7
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
46b32f46-6c90-4fd8-8453-05ea6d9d812e

Device Description

STRL SPONGE FORCEP

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
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
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
44058 General surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 10889942352012

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K884656 000