FDA UDI In Commercial Distribution 🇺🇸 United States

T-tube inserter

DI: 04250381805695 · Model: 1316012 · Spiggle & Theis Medizintechnik GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
T-tube inserter
Primary DI
04250381805695
Version / Model
1316012
Catalog Number
1316012
Company Name
Spiggle & Theis Medizintechnik GmbH
Labeler DUNS
332893028
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-16
Public Version
1
Public Version Date
2025-10-24
Public Version Status
New
Public Device Record Key
90a331fb-7689-4edd-b96a-494f333f2290

Device Description

not dismountable, for T-tubes in 6, 9 and 12 mm length

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
LRC INSTRUMENT, ENT MANUAL SURGICAL

GMDN Terms

Code Name
33404 Tympanostomy tube inserter, reusable

Identifiers

Type ID
Primary 04250381805695

Customer Contacts