FDA UDI Not in Commercial Distribution 🇺🇸 United States

TUOHY

DI: 04048223106969 · Model: 1150-6K091 · Pajunk GmbH Medizintechnologie
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
25

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Basic Information

Brand Name
TUOHY
Primary DI
04048223106969
Version / Model
1150-6K091
Catalog Number
1150-6K091
Company Name
Pajunk GmbH Medizintechnologie
Labeler DUNS
317654283
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2021-04-02
Public Version
5
Public Version Date
2025-12-01
Public Version Status
Update
Public Device Record Key
4868c2a0-83b7-496c-983d-534ac6db173a
Distribution End Date
2025-06-17

Device Description

Tuohy-Kanüle

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
BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

GMDN Terms

Code Name
58293 Epidural needle, non-threaded

Identifiers

Type ID
Unit of Use 04048223004012
Primary 04048223106969
Previous 14048223004019

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K040965 000

Device Sizes

Type Value Unit Text
Outer Diameter 1.3 Millimeter
Length 90.0 Millimeter

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 65 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
10 – 30 Degrees Celsius