FDA UDI In Commercial Distribution 🇺🇸 United States

Injection needle

DI: 04250676733757 · Model: 30-122-08 · Spiggle & Theis Medizintechnik GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Injection needle
Primary DI
04250676733757
Version / Model
30-122-08
Catalog Number
30-122-08
Company Name
Spiggle & Theis Medizintechnik GmbH
Labeler DUNS
332893028
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-19
Public Version
1
Public Version Date
2022-09-27
Public Version Status
New
Public Device Record Key
08f6b689-85a2-4049-b910-7c47b9f903e3

Device Description

angled, luer-lock 0.8 mm, wl 10.5 cm, total length 13 cm

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
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
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GDM NEEDLE, ASPIRATION AND INJECTION, REUSABLE

GMDN Terms

Code Name
46676 Tissue injection cannula

Identifiers

Type ID
Primary 04250676733757

Customer Contacts