FDA UDI In Commercial Distribution 🇺🇸 United States

Safety-Lancet Neonatal

DI: 04038917085069 · Model: 85.1019 · Sarstedt Aktiengesellschaft & Co.KG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
200

Basic Information

Brand Name
Safety-Lancet Neonatal
Primary DI
04038917085069
Version / Model
85.1019
Catalog Number
85.1019
Company Name
Sarstedt Aktiengesellschaft & Co.KG
Labeler DUNS
388000270
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2022-11-30
Public Version
2
Public Version Date
2023-02-01
Public Version Status
Update
Public Device Record Key
6fefe310-f32a-4586-85a9-8b966526dbf3

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
Yes
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
FMK Single use only blood lancet with an integral sharps injury prevention feature

GMDN Terms

Code Name
61578 Manual blood lancing device, single-use

Identifiers

Type ID
Unit of Use 04038917167185
Primary 04038917085069

Customer Contacts