FDA UDI In Commercial Distribution 🇺🇸 United States

SURFLO MIDELA

DI: 36927675520433 · Model: MCSD001F · Terumo Medical Products (Hangzhou) Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
20

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Basic Information

Brand Name
SURFLO MIDELA
Primary DI
36927675520433
Version / Model
MCSD001F
Catalog Number
MCSD001F
Company Name
Terumo Medical Products (Hangzhou) Co., Ltd.
Labeler DUNS
544830912
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2026-04-01
Public Version
1
Public Version Date
2026-04-09
Public Version Status
New
Public Device Record Key
3e63a8fc-2590-4611-b797-64fc66745a4d

Device Description

SURFLO MIDELA Securement Device

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KMK Device, Intravascular Catheter Securement

GMDN Terms

Code Name
56631 Wearable percutaneous catheter/tube holder, single-use

Identifiers

Type ID
Package 56927675520437
Primary 36927675520433
Unit of Use 06927675520432

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Do not store at extreme temperatures.Fragile, handle with care. Keep away from sunlight. Keep dry .Stacking limit by 5.