FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613327062908 · Model: 0502880214 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327062908
Version / Model
0502880214
Catalog Number
0502-880-214
Company Name
STRYKER CORPORATION
Labeler DUNS
187502109
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
9770bdc7-271c-4630-982e-772607c48347

Device Description

Rigid Optical Biopsy Forceps

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
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Hydrogen Peroxide", "Moist Heat or Steam Sterilization", "Ethylene Oxide"]

Product Codes

Code Name
HIH HYSTEROSCOPE (AND ACCESSORIES)

GMDN Terms

Code Name
17633 Urethrotome

Identifiers

Type ID
Primary 07613327062908

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Degree: 70.0 Degree