FDA UDI In Commercial Distribution 🇺🇸 United States

Multifly®-Needle

DI: 04038917423755 · Model: 85.1638.001 · Sarstedt Aktiengesellschaft & Co.KG
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
120

Basic Information

Brand Name
Multifly®-Needle
Primary DI
04038917423755
Version / Model
85.1638.001
Catalog Number
85.1638.001
Company Name
Sarstedt Aktiengesellschaft & Co.KG
Labeler DUNS
388000270
Distribution Status
In Commercial Distribution
Device Count in Pkg
120
Record Status
Published
Publish Date
2019-10-06
Public Version
4
Public Version Date
2020-07-23
Public Version Status
Update
Public Device Record Key
a27fcc8e-9daf-4f6b-9131-14a0738f5e13

Device Description

Multifly®Needle 21G tube 200mm without adapter

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
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
FPA Set, Administration, Intravascular
JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

GMDN Terms

Code Name
58490 Venous butterfly needle/set

Identifiers

Type ID
Primary 04038917423755
Unit of Use 04038917204668

Customer Contacts