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OBTURATOR, Ø3.6mm

FDA UDI

Class II (US FDA UDI)

by Advanced Orthopaedic Solutions, Inc.

Identity

Trade Name
OBTURATOR, Ø3.6mm FDA UDI
Generic Name
Surgical drill guide obturator FDA UDI
Model / Reference
0227-000 FDA UDI

Identifiers

Primary DI / UDI-DI
00848665000696 FDA UDI
510(k) Number
K014185 FDA UDI
K021008 FDA UDI
K070444 FDA UDI
FDA Product Code
HSB FDA UDI
HWC FDA UDI
GMDN Term
Surgical drill guide obturator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical drill guide obturator

OBTURATOR, Ø3.6mm by Advanced Orthopaedic Solutions, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical drill guide obturator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c0527ac6-1efe-4520-811f-bb020b13331e 34 fields · synced Jun 8, 2026