FDA UDI In Commercial Distribution 🇺🇸 United States

Adler Instrument Company

DI: 00810123203307 · Model: 36-0201 · Adler, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Adler Instrument Company
Primary DI
00810123203307
Version / Model
36-0201
Company Name
Adler, Inc.
Labeler DUNS
830141235
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-09
Public Version
1
Public Version Date
2023-03-17
Public Version Status
New
Public Device Record Key
2e39c5c0-b620-47ce-9078-f8920cc92515

Device Description

PUTTI RASP 10-3/4 FLT BLD

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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GAC Rasp, Surgical, General & Plastic Surgery

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary 00810123203307

Customer Contacts

Phone
8772416747