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Blue Sky Bio, LLC.

FDA UDI

Class I (US FDA UDI)

by Blue Sky Bio Llc

Identity

Trade Name
Blue Sky Bio, LLC. FDA UDI
Generic Name
Fixture/appliance dental drill bit, reusable FDA UDI
Device Name
Guided Drill Narrow 3.0 x 8.0mm FDA UDI
Model / Reference
DRILGN3008 FDA UDI
Description
Guided Drill Narrow 3.0 x 8.0mm FDA UDI

Identifiers

Primary DI / UDI-DI
00810060225332 FDA UDI
FDA Product Code
EBL FDA UDI
GMDN Term
Fixture/appliance dental drill bit, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3740 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

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: Fixture/appliance dental drill bit, reusable

Blue Sky Bio, LLC. by Blue Sky Bio Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fixture/appliance dental drill bit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Blue Sky Bio Llc

Sources (1)

  • FDA UDI d78b34ca-2db1-4ed3-8b95-9b6a2b3e2dca 33 fields · synced Jun 1, 2026