FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10887587025919 · Model: 05.725.010 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10887587025919
Version / Model
05.725.010
Catalog Number
05725010
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-12-03
Public Version
4
Public Version Date
2022-04-25
Public Version Status
Update
Public Device Record Key
aee1f3e4-2a63-4cc0-8e3c-4d85d57b8ec9

Device Description

COMPACT WATER BATH

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
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JTQ BATH, INCUBATORS/WATER, ALL

GMDN Terms

Code Name
47744 Surgical water bath system

Identifiers

Type ID
Secondary H9800572501009
Primary 10887587025919
Direct Marking 07611819618060

Customer Contacts