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Aseptico Technique

FDA UDI

Class I (US FDA UDI)

by Aseptico, Inc.

Identity

Trade Name
Aseptico Technique FDA UDI
Generic Name
Orthodontic wire FDA UDI
Device Name
KIT BICUSPID CHAIN / GRID FDA UDI
Model / Reference
AMA-09A2 FDA UDI
Description
KIT BICUSPID CHAIN / GRID FDA UDI

Identifiers

Primary DI / UDI-DI
10817417021811 FDA UDI
FDA Product Code
DZC FDA UDI
GMDN Term
Orthodontic wire FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5410 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

Category: Orthodontic wire

Aseptico Technique by Aseptico, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic wire.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aseptico, Inc.

Sources (1)

  • FDA UDI 73848fd4-b22a-4764-afda-22c99766789a 34 fields · synced May 30, 2026