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Lithotomy Pack *RFID PB

FDA UDI

by Packroom Llc

Identity

Trade Name
Lithotomy Pack *RFID PB FDA UDI
Generic Name
General surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
Lithotomy Pack *RFID PB FDA UDI
Model / Reference
DYNJ84454-V.1RFPB FDA UDI
Description
Lithotomy Pack *RFID PB FDA UDI

Identifiers

Primary DI / UDI-DI
00817395023831 FDA UDI
GMDN Term
General surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

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

No

FDA UDI

Category: General surgical procedure kit, non-medicated, single-use

Lithotomy Pack *RFID PB by Packroom Llc — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General surgical procedure kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Packroom Llc

Sources (1)

  • FDA UDI 6ddb2378-8916-4352-ad2c-58f1704b3a65 33 fields · synced Jun 1, 2026