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Straight Abutment Transfer (2 pieces)

FDA UDI

Class I (US FDA UDI)

by Implant Direct Sybron Manufacturing Llc

Identity

Trade Name
Straight Abutment Transfer (2 pieces) FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Model / Reference
3037-02 FDA UDI

Identifiers

Catalog Number
3037-02 FDA UDI
Primary DI / UDI-DI
10841307121022 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant suprastructure, temporary, preformed, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant suprastructure, temporary, preformed, single-use

A comprehensive and accurate directory listing for the Straight Abutment Transfer (2 pieces), a medical device used during dental implant restorative and laboratory procedures. Our expert team has carefully reviewed and verified this information to ensure it meets the highest standards of accuracy and compliance.

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Implant Direct Sybron Manufacturing Llc

Sources (1)

  • FDA UDI 91f47d8d-540e-4b3b-8720-d630a9d36364 35 fields · synced Jul 9, 2026