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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
Instrument tray, reusable FDA UDI
Device Name
BIO | TAD Nest FDA UDI
Model / Reference
TADNEST FDA UDI
Description
BIO | TAD Nest FDA UDI

Identifiers

Primary DI / UDI-DI
00810060225516 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Instrument tray, reusable 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

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, 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 Instrument tray, 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 03448546-0b4e-4b5d-86af-2ddd4e0a8cef 33 fields · synced Jun 1, 2026