FDA UDI In Commercial Distribution 🇺🇸 United States

Immucise

DI: 34987892133023 · Model: IE-D102US · TERUMO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

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Basic Information

Brand Name
Immucise
Primary DI
34987892133023
Version / Model
IE-D102US
Company Name
TERUMO CORPORATION
Labeler DUNS
690543319
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2025-06-13
Public Version
1
Public Version Date
2025-06-23
Public Version Status
New
Public Device Record Key
38b08e1b-d52f-4dad-8532-846d36cc6adf

Device Description

Immucise Syringe

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMF Syringe, piston

GMDN Terms

Code Name
63095 General-purpose syringe/needle

Identifiers

Type ID
Package 54987892133027
Primary 34987892133023
Unit of Use 04987892133022

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 0.4 Milliliter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry and keep away from sunlight.
Type
Special Storage Condition, Specify
Special Conditions
Store at temperature between 2 and 50 Celcius Degrees.