FDA UDI In Commercial Distribution 🇺🇸 United States

Forceps holder

DI: 04250381892084 · Model: 80-528-20 · Spiggle & Theis Medizintechnik GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Forceps holder
Primary DI
04250381892084
Version / Model
80-528-20
Catalog Number
80-528-20
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
99db6e06-79f4-4e7f-b54b-8412616d8d8f

Device Description

stainless steel Ø 95 mm, height 200 mm

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
62851 Surgical instrument interim-placement holder, reusable

Identifiers

Type ID
Primary 04250381892084

Customer Contacts