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Phoebe Main LTC GYN Lap Pack LF

FDA UDI

by Packroom Llc

Identity

Trade Name
Phoebe Main LTC GYN Lap Pack LF FDA UDI
Generic Name
Laparoscopic surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
Phoebe Main LTC GYN Lap Pack LF FDA UDI
Model / Reference
PM220 FDA UDI
Description
Phoebe Main LTC GYN Lap Pack LF FDA UDI

Identifiers

Primary DI / UDI-DI
00817395020632 FDA UDI
GMDN Term
Laparoscopic 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: Laparoscopic surgical procedure kit, non-medicated, single-use

Phoebe Main LTC GYN Lap Pack LF by Packroom Llc — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laparoscopic 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 f29db9cd-9ea0-4baf-8ff2-24a0b1cbd50d 33 fields · synced May 31, 2026