FDA UDI In Commercial Distribution 🇺🇸 United States

Provox FenestrationPunch

DI: 07331791002632 · Model: 7654 · Atos Medical AB
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Provox FenestrationPunch
Primary DI
07331791002632
Version / Model
7654
Catalog Number
7654
Company Name
Atos Medical AB
Labeler DUNS
355470923
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-25
Public Version
1
Public Version Date
2022-12-05
Public Version Status
New
Public Device Record Key
229af426-0c5a-4948-af60-7775305e98c9

Device Description

The Fenestration Punch is used for making small fenestrations in a Provox LaryTube at desired locations.

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
No
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
KTF Punch, Ent

GMDN Terms

Code Name
38792 Tracheostomy tube, non-reinforced, non-customized, reusable

Identifiers

Type ID
Primary 07331791002632

Customer Contacts

Phone
+4641519800

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 42 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
36 – 108 Degrees Fahrenheit
Type
Special Storage Condition, Specify
Special Conditions
Keep dry. Keep away from sunlight