FDA UDI In Commercial Distribution 🇺🇸 United States

Inflation device

DI: 04250676743473 · Model: 2080-9030040-US · Spiggle & Theis Medizintechnik GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Inflation device
Primary DI
04250676743473
Version / Model
2080-9030040-US
Catalog Number
2080-9030040-US
Company Name
Spiggle & Theis Medizintechnik GmbH
Labeler DUNS
332893028
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-07
Public Version
1
Public Version Date
2023-09-15
Public Version Status
New
Public Device Record Key
810d4d40-92c0-45b6-acea-398b212d141e

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
No
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
No

Product Codes

Code Name
PNZ Eustachian tube balloon dilation device

GMDN Terms

Code Name
17541 Catheter/overtube balloon inflator, single-use

Identifiers

Type ID
Primary 04250676743473

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K223542 000