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Stents Removal Forceps-Working Length 60cm

FDA UDI

Class I (US FDA UDI)

by Iaa Surgical Instruments Company

Identity

Trade Name
STENTS REMOVAL FORCEPS-WORKING LENGTH 60CM FDA UDI
Generic Name
Bronchoscopic biopsy curette, flexible, reusable FDA UDI
Model / Reference
BPS2003 FDA UDI

Identifiers

Catalog Number
BPS2003 FDA UDI
Primary DI / UDI-DI
B832BPS20030 FDA UDI
FDA Product Code
HTD FDA UDI
GMDN Term
Bronchoscopic biopsy curette, flexible, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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

No

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: Bronchoscopic biopsy curette, flexible, reusable

Stents Removal Forceps-Working Length 60cm by Iaa Surgical Instruments Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bronchoscopic biopsy curette, flexible, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3140994b-44fc-4aa6-abff-1e841b55d9fc 33 fields · synced Jun 1, 2026