NNC CEMENTABLE ABUTMENT STRAIGHT,15 DEGREE ANGLE, 048.257

GUDID 07630031723833

NNC Plastic coping, for 048.598, for bridge, H 7mm, POM

Institut Straumann AG

Dental implant suprastructure, temporary, preformed, single-use

Primary Device ID	07630031723833
NIH Device Record Key	1932085f-c6d2-4bb3-ad97-9d7837c94a4b
Commercial Distribution Status	In Commercial Distribution
Brand Name	NNC CEMENTABLE ABUTMENT STRAIGHT,15 DEGREE ANGLE,
Version Model Number	1
Catalog Number	048.257
Company DUNS	483599259
Company Name	Institut Straumann AG
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Customer Support Contacts

Phone	+1(800)448-8168
Email	info.usa@straumann.com
Phone	+1(800)448-8168
Email	info.usa@straumann.com
Phone	+1(800)448-8168
Email	info.usa@straumann.com
Phone	+1(800)448-8168
Email	info.usa@straumann.com
Phone	+1(800)448-8168
Email	info.usa@straumann.com
Phone	+1(800)448-8168
Email	info.usa@straumann.com
Phone	+1(800)448-8168
Email	info.usa@straumann.com
Phone	+1(800)448-8168
Email	info.usa@straumann.com
Phone	+1(800)448-8168
Email	info.usa@straumann.com
Phone	+1(800)448-8168
Email	info.usa@straumann.com
Phone	+1(800)448-8168
Email	info.usa@straumann.com
Phone	+1(800)448-8168
Email	info.usa@straumann.com
Phone	+1(800)448-8168
Email	info.usa@straumann.com
Phone	+1(800)448-8168
Email	info.usa@straumann.com
Phone	+1(800)448-8168
Email	info.usa@straumann.com
Phone	+1(800)448-8168
Email	info.usa@straumann.com
Phone	+1(800)448-8168
Email	info.usa@straumann.com
Phone	+1(800)448-8168
Email	info.usa@straumann.com
Phone	+1(800)448-8168
Email	info.usa@straumann.com

Operating and Storage Conditions

Special Storage Condition, Specify	Between 0 and 0 *Keep away from light and sun
Special Storage Condition, Specify	Between 0 and 0 *Keep away from light and sun
Special Storage Condition, Specify	Between 0 and 0 *Keep away from light and sun
Special Storage Condition, Specify	Between 0 and 0 *Keep away from light and sun
Special Storage Condition, Specify	Between 0 and 0 *Keep away from light and sun
Special Storage Condition, Specify	Between 0 and 0 *Keep away from light and sun
Special Storage Condition, Specify	Between 0 and 0 *Keep away from light and sun
Special Storage Condition, Specify	Between 0 and 0 *Keep away from light and sun
Special Storage Condition, Specify	Between 0 and 0 *Keep away from light and sun
Special Storage Condition, Specify	Between 0 and 0 *Keep away from light and sun
Special Storage Condition, Specify	Between 0 and 0 *Keep away from light and sun
Special Storage Condition, Specify	Between 0 and 0 *Keep away from light and sun
Special Storage Condition, Specify	Between 0 and 0 *Keep away from light and sun
Special Storage Condition, Specify	Between 0 and 0 *Keep away from light and sun
Special Storage Condition, Specify	Between 0 and 0 *Keep away from light and sun
Special Storage Condition, Specify	Between 0 and 0 *Keep away from light and sun
Special Storage Condition, Specify	Between 0 and 0 *Keep away from light and sun
Special Storage Condition, Specify	Between 0 and 0 *Keep away from light and sun
Special Storage Condition, Specify	Between 0 and 0 *Keep away from light and sun

Device Identifiers

Device Issuing Agency	Device ID
GS1	07630031723833 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K113283

FDA Product Code

NDP	ACCESSORIES, IMPLANT, DENTAL, ENDOSSEOUS