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Reservoir Bag

FDA UDI

Class I (US FDA UDI)

by Typenex Medical, LLC

Identity

Trade Name
Reservoir Bag FDA UDI
Generic Name
Blood irradiation indicator FDA UDI
Device Name
Anesthesia Reservoir Bag, 3L FDA UDI
Model / Reference
LF3 FDA UDI
Description
Anesthesia Reservoir Bag, 3L FDA UDI

Identifiers

Primary DI / UDI-DI
00810050854146 FDA UDI
FDA Product Code
BTC FDA UDI
GMDN Term
Blood irradiation indicator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5320 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

No

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blood irradiation indicator

Reservoir Bag by Typenex Medical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood irradiation indicator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9384ee0c-3f22-42c2-85f9-fd6f086b41b5 33 fields · synced May 31, 2026